• Je něco špatně v tomto záznamu ?

The landscape of epilepsy-related GATOR1 variants

S. Baldassari, F. Picard, NE. Verbeek, M. van Kempen, EH. Brilstra, G. Lesca, V. Conti, R. Guerrini, F. Bisulli, L. Licchetta, T. Pippucci, P. Tinuper, E. Hirsch, A. de Saint Martin, J. Chelly, G. Rudolf, M. Chipaux, S. Ferrand-Sorbets, G....

. 2019 ; 21 (2) : 398-408. [pub] 20180810

Jazyk angličtina Země Spojené státy americké

Typ dokumentu časopisecké články, práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/bmc19028279

Grantová podpora
682345 European Research Council - International
K12 NS098482 NINDS NIH HHS - United States

PURPOSE: To define the phenotypic and mutational spectrum of epilepsies related to DEPDC5, NPRL2 and NPRL3 genes encoding the GATOR1 complex, a negative regulator of the mTORC1 pathway METHODS: We analyzed clinical and genetic data of 73 novel probands (familial and sporadic) with epilepsy-related variants in GATOR1-encoding genes and proposed new guidelines for clinical interpretation of GATOR1 variants. RESULTS: The GATOR1 seizure phenotype consisted mostly in focal seizures (e.g., hypermotor or frontal lobe seizures in 50%), with a mean age at onset of 4.4 years, often sleep-related and drug-resistant (54%), and associated with focal cortical dysplasia (20%). Infantile spasms were reported in 10% of the probands. Sudden unexpected death in epilepsy (SUDEP) occurred in 10% of the families. Novel classification framework of all 140 epilepsy-related GATOR1 variants (including the variants of this study) revealed that 68% are loss-of-function pathogenic, 14% are likely pathogenic, 15% are variants of uncertain significance and 3% are likely benign. CONCLUSION: Our data emphasize the increasingly important role of GATOR1 genes in the pathogenesis of focal epilepsies (>180 probands to date). The GATOR1 phenotypic spectrum ranges from sporadic early-onset epilepsies with cognitive impairment comorbidities to familial focal epilepsies, and SUDEP.

Bethel Epilepsy Centre Bielefeld Germany

Centre de Référence Anomalies du Développement et Syndromes Malformatifs et FHU TRANSLAD CHU de Dijon et Université de Bourgogne Dijon France

Centre Hospitalier Universitaire de Rennes F 35000 Rennes France

Children's Hospital Los Angeles Keck School of Medicine University of Southern California Los Angeles California USA

CHU Reims American Memorial Hospital Service de Pédiatrie REIMS F 51092 France

CHU Reims Hôpital Maison Blanche Pôle de Biologie Service de Génétique Reims F 51092 France

Clinique Bernoise Crans Montana Switzerland

CNRS UMR 5292 INSERM U1028 CNRL et Université Claude Bernard Lyon 1 GHE Lyon France

Danish Epilepsy Centre Dianalund

Danish Epilepsy Centre Dianalund Denmark

Danish Epilepsy Centre Dianalund University of Copenhagen Copenhagen Denmark

Department of Biomedical and Neuromotor Sciences University of Bologna Bologna Italy

Department of Child Neurology Brain Center Rudolf Magnus University Medical Center Utrecht The Netherlands

Department of Clinical and Experimental Epilepsy UCL Institute of Neurology WC1N 3BG and Chalfont Centre for Epilepsy Bucks UK

Department of Clinical Neurosciences University Hospitals and Medical School of Geneva Geneva Switzerland

Department of Genetics University Medical Center Utrecht Utrecht The Netherlands

Department of Medicine Divisions of Neurology and Respirology Queen's University Kingston Ontario Canada Kingston Health Sciences Centre Kingston Ontario K7L 2V7 Canada

Department of Neurology Academic Center for Epileptology Kempenhaeghe Heeze The Netherlands

Department of Neurology and Rehabilitation Tallinn Children's Hospital Tallinn Estonia

Department of Neurology centre de référence des épilepsies rares University Hospital of Strasbourg Strasbourg France

Department of Neurology F M Kirby Neurobiology Center Boston Children's Hospital Boston Massachusetts USA Division of Epilepsy and Clinical Neurophysiology and Epilepsy Genetics Program Boston Children's Hospital Boston Massachusetts USA Department of Neurology Harvard Medical School Boston Massachusetts USA

Department of Paediatric Neurology Motol University Hospital 2nd faculty of medicine Charles University Prague Czech Republic

Department of Pediatric Neurology and Developmental Medicine University Children's Hospital Tübingen Germany

Department of Pediatric Neurology Antwerp University Hospital Edegem Belgium

Department of Pediatric Neurology Children's Hospital Datteln Witten Herdecke University Datteln Germany

Department of Pediatric Neurology Rady Children's Hospital University of California San Diego California USA

Department of Pediatric Neurosurgery Fondation Rothschild F 75019 Paris France

Department of Pediatrics centre de référence des épilepsies rares University Hospital of Strasbourg Strasbourg France

Department of Pediatrics Institute of Medicine University Hospital of Udine Udine Italy

Division of Genetics and Metabolism Phoenix Children's Hospital Phoenix Arizona USA

Epilepsy Center Clinic of Nervous System Diseases University of Foggia Riuniti Hospital Foggia Italy

Epilepsy Center for Children Brandenburg Medical School University Hospital Neuruppin Germany

IGBMC INSERM CNRS Strasbourg University Strasbourg France

Inserm UMR 1231 GAD Team Genetics of Developmental Anomalies et FHU TRANSLAD CHU Université de Bourgogne Franche Comté Dijon France

Institut de Systématique Evolution Biodiversité ISYEB UMR 7205 CNRS MNHN UPMC EPHE Paris France

Institute for Regional Health research University of Southern Denmark Odense Denmark

Institute of Human Genetics University Hospital Magdeburg Germany

Institute of Human Genetics University of Leipzig Hospitals and Clinics Leipzig Germany

Institute of Neurology Department of Medical and Surgical Sciences University Magna Græcia Catanzaro Italy

IRCCS Istituto delle Scienze Neurologiche of Bologna

Kinderneurologisches Zentrum Düsseldorf Gerresheim Sana Kliniken Düsseldorf Germany

Kingston Health Sciences Centre Kingston Ontario K7L 2V7 Canada

Leiden University Medical Center Leiden The Netherlands

Medical Genetics Unit Polyclinic Sant' Orsola Malpighi University Hospital Bologna Italy

Neurogenetics Group VIB Department of Molecular Genetics University of Antwerp Antwerp Belgium

Paediatric Clinical Epileptology Sleep disorders and Functional Neurology University Hospitals of Lyon Lyon France

Pediatric Neurology and Muscular Diseases Unit Department of Neurosciences Rehabilitation Ophthalmology Genetics Maternal and Child Health University of Genoa G Gaslini Institute Genova Italy

Pediatric Neurology Department Timone Hospital APHM Marseille France

Pediatric Neurology Neurogenetics and Neurobiology Unit and Laboratories A Meyer Children's Hospital Florence Italy

Service d'Epileptologie Clinique CHU de Bordeaux France

Service de Génétique Hospices Civils de Lyon GHE

Service de Génétique Médicale Pavillon Lefebvre Hôpital Purpan CHU Toulouse Toulouse France

Service de neurophysiologie et pédiatrie 1 CHU de Dijon Dijon France

Sorbonne Université UPMC Univ Paris 06 UMR S 1127 F 75013 Paris France INSERM U1127 F 75013 Paris France CNRS UMR 7225 F 75013 Paris France Institut du Cerveau et de la Moelle épinière Hôpital Pitié Salpêtrière F 75013 Paris France

Stichting Epilepsie Instellingen Nederland Zwolle Heemstede The Netherlands

The Saxon Epilepsy Center Kleinwachau Radeberg Germany

Unit of Medical Genetics CHU La Réunion Saint Pierre F 97448 France

Unité d'épileptologie Service de Neurologie CHU 49033 Angers France

Vrije Universiteit Brussel Neurogenetics Research Group Laarbeeklaan 101 1090 Brussels Belgium

Citace poskytuje Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc19028279
003      
CZ-PrNML
005      
20190819113446.0
007      
ta
008      
190813s2019 xxu f 000 0|eng||
009      
AR
024    7_
$a 10.1038/s41436-018-0060-2 $2 doi
035    __
$a (PubMed)30093711
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a xxu
100    1_
$a Baldassari, Sara $u Sorbonne Université, UPMC Univ Paris 06, UMR S 1127, F-75013, Paris, France. INSERM, U1127, F-75013, Paris, France. CNRS, UMR 7225, F-75013, Paris, France. Institut du Cerveau et de la Moelle épinière (ICM), Hôpital Pitié-Salpêtrière, F-75013, Paris, France. Department of Genetics, Assistance Publique des Hôpitaux de Paris (AP-HP), Hôpital Pitié-Salpêtrière, F-75013, Paris, France.
245    14
$a The landscape of epilepsy-related GATOR1 variants / $c S. Baldassari, F. Picard, NE. Verbeek, M. van Kempen, EH. Brilstra, G. Lesca, V. Conti, R. Guerrini, F. Bisulli, L. Licchetta, T. Pippucci, P. Tinuper, E. Hirsch, A. de Saint Martin, J. Chelly, G. Rudolf, M. Chipaux, S. Ferrand-Sorbets, G. Dorfmüller, S. Sisodiya, S. Balestrini, N. Schoeler, L. Hernandez-Hernandez, S. Krithika, R. Oegema, E. Hagebeuk, B. Gunning, C. Deckers, B. Berghuis, I. Wegner, E. Niks, FE. Jansen, K. Braun, D. de Jong, G. Rubboli, I. Talvik, V. Sander, P. Uldall, ML. Jacquemont, C. Nava, E. Leguern, S. Julia, A. Gambardella, G. d'Orsi, G. Crichiutti, L. Faivre, V. Darmency, B. Benova, P. Krsek, A. Biraben, AS. Lebre, M. Jennesson, S. Sattar, C. Marchal, DR. Nordli, K. Lindstrom, P. Striano, LB. Lomax, C. Kiss, F. Bartolomei, AF. Lepine, AS. Schoonjans, K. Stouffs, A. Jansen, E. Panagiotakaki, B. Ricard-Mousnier, J. Thevenon, J. de Bellescize, H. Catenoix, T. Dorn, M. Zenker, K. Müller-Schlüter, C. Brandt, I. Krey, T. Polster, M. Wolff, M. Balci, K. Rostasy, G. Achaz, P. Zacher, T. Becher, T. Cloppenborg, CJ. Yuskaitis, S. Weckhuysen, A. Poduri, JR. Lemke, RS. Møller, S. Baulac,
520    9_
$a PURPOSE: To define the phenotypic and mutational spectrum of epilepsies related to DEPDC5, NPRL2 and NPRL3 genes encoding the GATOR1 complex, a negative regulator of the mTORC1 pathway METHODS: We analyzed clinical and genetic data of 73 novel probands (familial and sporadic) with epilepsy-related variants in GATOR1-encoding genes and proposed new guidelines for clinical interpretation of GATOR1 variants. RESULTS: The GATOR1 seizure phenotype consisted mostly in focal seizures (e.g., hypermotor or frontal lobe seizures in 50%), with a mean age at onset of 4.4 years, often sleep-related and drug-resistant (54%), and associated with focal cortical dysplasia (20%). Infantile spasms were reported in 10% of the probands. Sudden unexpected death in epilepsy (SUDEP) occurred in 10% of the families. Novel classification framework of all 140 epilepsy-related GATOR1 variants (including the variants of this study) revealed that 68% are loss-of-function pathogenic, 14% are likely pathogenic, 15% are variants of uncertain significance and 3% are likely benign. CONCLUSION: Our data emphasize the increasingly important role of GATOR1 genes in the pathogenesis of focal epilepsies (>180 probands to date). The GATOR1 phenotypic spectrum ranges from sporadic early-onset epilepsies with cognitive impairment comorbidities to familial focal epilepsies, and SUDEP.
650    _2
$a mladiství $7 D000293
650    _2
$a Brugadův syndrom $x genetika $x mortalita $x patofyziologie $7 D053840
650    _2
$a dítě $7 D002648
650    _2
$a předškolní dítě $7 D002675
650    _2
$a variabilita počtu kopií segmentů DNA $x genetika $7 D056915
650    _2
$a epilepsie $x komplikace $x epidemiologie $x genetika $x patofyziologie $7 D004827
650    _2
$a ženské pohlaví $7 D005260
650    _2
$a proteiny aktivující GTPasu $x genetika $7 D020690
650    _2
$a genetická predispozice k nemoci $7 D020022
650    _2
$a lidé $7 D006801
650    _2
$a mutace INDEL $x genetika $7 D054643
650    _2
$a kojenec $7 D007223
650    _2
$a novorozenec $7 D007231
650    _2
$a mutace ztráty funkce $x genetika $7 D000073658
650    _2
$a mužské pohlaví $7 D008297
650    _2
$a mTORC1 $x genetika $7 D000076222
650    _2
$a multiproteinové komplexy $x genetika $7 D046912
650    _2
$a rodokmen $7 D010375
650    _2
$a represorové proteiny $x genetika $7 D012097
650    _2
$a záchvaty $x komplikace $x epidemiologie $x genetika $x patofyziologie $7 D012640
650    _2
$a signální transdukce $x genetika $7 D015398
650    _2
$a nádorové supresorové proteiny $x genetika $7 D025521
655    _2
$a časopisecké články $7 D016428
655    _2
$a práce podpořená grantem $7 D013485
700    1_
$a Picard, Fabienne $u Department of Clinical Neurosciences, University Hospitals and Medical School of Geneva, Geneva, Switzerland.
700    1_
$a Verbeek, Nienke E $u Department of Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.
700    1_
$a van Kempen, Marjan $u Department of Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.
700    1_
$a Brilstra, Eva H $u Department of Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.
700    1_
$a Lesca, Gaetan $u Service de Génétique, Hospices Civils de Lyon - GHE; CNRS UMR 5292, INSERM U1028, CNRL, et Université Claude Bernard Lyon 1, GHE, Lyon, France.
700    1_
$a Conti, Valerio $u Pediatric Neurology, Neurogenetics, and Neurobiology Unit and Laboratories, A. Meyer Children's Hospital, Florence, Italy.
700    1_
$a Guerrini, Renzo $u Pediatric Neurology, Neurogenetics, and Neurobiology Unit and Laboratories, A. Meyer Children's Hospital, Florence, Italy.
700    1_
$a Bisulli, Francesca $u IRCCS, Istituto delle Scienze Neurologiche of Bologna; Department of Biomedical and Neuromotor Sciences, University of Bologna, Bologna, Italy.
700    1_
$a Licchetta, Laura $u IRCCS, Istituto delle Scienze Neurologiche of Bologna; Department of Biomedical and Neuromotor Sciences, University of Bologna, Bologna, Italy.
700    1_
$a Pippucci, Tommaso $u Medical Genetics Unit, Polyclinic Sant' Orsola-Malpighi University Hospital, Bologna, Italy.
700    1_
$a Tinuper, Paolo $u IRCCS, Istituto delle Scienze Neurologiche of Bologna; Department of Biomedical and Neuromotor Sciences, University of Bologna, Bologna, Italy.
700    1_
$a Hirsch, Edouard $u Department of Neurology-centre de référence des épilepsies rares, University Hospital of Strasbourg, Strasbourg, France.
700    1_
$a de Saint Martin, Anne $u Department of Pediatrics - centre de référence des épilepsies rares, University Hospital of Strasbourg, Strasbourg, France.
700    1_
$a Chelly, Jamel $u IGBMC, INSERM, CNRS, Strasbourg University, Strasbourg, France.
700    1_
$a Rudolf, Gabrielle $u IGBMC, INSERM, CNRS, Strasbourg University, Strasbourg, France.
700    1_
$a Chipaux, Mathilde $u Department of Pediatric Neurosurgery, Fondation Rothschild, F-75019, Paris, France.
700    1_
$a Ferrand-Sorbets, Sarah $u Department of Pediatric Neurosurgery, Fondation Rothschild, F-75019, Paris, France.
700    1_
$a Dorfmüller, Georg $u Department of Pediatric Neurosurgery, Fondation Rothschild, F-75019, Paris, France.
700    1_
$a Sisodiya, Sanjay $u Department of Clinical and Experimental Epilepsy, UCL Institute of Neurology, WC1N 3BG, and Chalfont Centre for Epilepsy, Bucks, UK.
700    1_
$a Balestrini, Simona $u Department of Clinical and Experimental Epilepsy, UCL Institute of Neurology, WC1N 3BG, and Chalfont Centre for Epilepsy, Bucks, UK.
700    1_
$a Schoeler, Natasha $u Department of Clinical and Experimental Epilepsy, UCL Institute of Neurology, WC1N 3BG, and Chalfont Centre for Epilepsy, Bucks, UK.
700    1_
$a Hernandez-Hernandez, Laura $u Department of Clinical and Experimental Epilepsy, UCL Institute of Neurology, WC1N 3BG, and Chalfont Centre for Epilepsy, Bucks, UK.
700    1_
$a Krithika, S $u Department of Clinical and Experimental Epilepsy, UCL Institute of Neurology, WC1N 3BG, and Chalfont Centre for Epilepsy, Bucks, UK.
700    1_
$a Oegema, Renske $u Department of Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.
700    1_
$a Hagebeuk, Eveline $u Stichting Epilepsie Instellingen Nederland, Zwolle/Heemstede, The Netherlands.
700    1_
$a Gunning, Boudewijn $u Stichting Epilepsie Instellingen Nederland, Zwolle/Heemstede, The Netherlands.
700    1_
$a Deckers, Charles $u Stichting Epilepsie Instellingen Nederland, Zwolle/Heemstede, The Netherlands.
700    1_
$a Berghuis, Bianca $u Stichting Epilepsie Instellingen Nederland, Zwolle/Heemstede, The Netherlands.
700    1_
$a Wegner, Ilse $u Stichting Epilepsie Instellingen Nederland, Zwolle/Heemstede, The Netherlands.
700    1_
$a Niks, Erik $u Leiden University Medical Center, Leiden, The Netherlands.
700    1_
$a Jansen, Floor E $u Department of Child Neurology, Brain Center Rudolf Magnus, University Medical Center, Utrecht, The Netherlands.
700    1_
$a Braun, Kees $u Department of Child Neurology, Brain Center Rudolf Magnus, University Medical Center, Utrecht, The Netherlands.
700    1_
$a de Jong, Daniëlle $u Department of Neurology, Academic Center for Epileptology Kempenhaeghe, Heeze, The Netherlands.
700    1_
$a Rubboli, Guido $u Danish Epilepsy Centre, Dianalund, University of Copenhagen, Copenhagen, Denmark.
700    1_
$a Talvik, Inga $u Department of Neurology and Rehabilitation, Tallinn Children's Hospital, Tallinn, Estonia.
700    1_
$a Sander, Valentin $u Department of Neurology and Rehabilitation, Tallinn Children's Hospital, Tallinn, Estonia.
700    1_
$a Uldall, Peter $u Danish Epilepsy Centre, Dianalund, Denmark.
700    1_
$a Jacquemont, Marie-Line $u Unit of Medical Genetics, CHU La Réunion, Saint Pierre, F-97448, France.
700    1_
$a Nava, Caroline $u Sorbonne Université, UPMC Univ Paris 06, UMR S 1127, F-75013, Paris, France. INSERM, U1127, F-75013, Paris, France. CNRS, UMR 7225, F-75013, Paris, France. Institut du Cerveau et de la Moelle épinière (ICM), Hôpital Pitié-Salpêtrière, F-75013, Paris, France. Department of Genetics, Assistance Publique des Hôpitaux de Paris (AP-HP), Hôpital Pitié-Salpêtrière, F-75013, Paris, France.
700    1_
$a Leguern, Eric $u Sorbonne Université, UPMC Univ Paris 06, UMR S 1127, F-75013, Paris, France. INSERM, U1127, F-75013, Paris, France. CNRS, UMR 7225, F-75013, Paris, France. Institut du Cerveau et de la Moelle épinière (ICM), Hôpital Pitié-Salpêtrière, F-75013, Paris, France. Department of Genetics, Assistance Publique des Hôpitaux de Paris (AP-HP), Hôpital Pitié-Salpêtrière, F-75013, Paris, France.
700    1_
$a Julia, Sophie $u Service de Génétique Médicale, Pavillon Lefebvre, Hôpital Purpan CHU Toulouse, Toulouse, France.
700    1_
$a Gambardella, Antonio $u Institute of Neurology, Department of Medical and Surgical Sciences, University Magna Græcia, Catanzaro, Italy.
700    1_
$a d'Orsi, Giuseppe $u Epilepsy Center, Clinic of Nervous System Diseases, University of Foggia, Riuniti Hospital, Foggia, Italy.
700    1_
$a Crichiutti, Giovanni $u Department of Pediatrics, Institute of Medicine, University Hospital of Udine, Udine, Italy.
700    1_
$a Faivre, Laurence $u Centre de Référence Anomalies du Développement et Syndromes Malformatifs et FHU TRANSLAD, CHU de Dijon et Université de Bourgogne, Dijon, France.
700    1_
$a Darmency, Veronique $u Service de neurophysiologie et pédiatrie 1, CHU de Dijon, Dijon, France.
700    1_
$a Benova, Barbora $u Department of Paediatric Neurology, Motol University Hospital, 2nd faculty of medicine Charles University, Prague, Czech Republic.
700    1_
$a Krsek, Pavel $u Department of Paediatric Neurology, Motol University Hospital, 2nd faculty of medicine Charles University, Prague, Czech Republic.
700    1_
$a Biraben, Arnaud $u Centre Hospitalier Universitaire de Rennes, F-35000, Rennes, France.
700    1_
$a Lebre, Anne-Sophie $u CHU Reims, Hôpital Maison Blanche, Pôle de Biologie, Service de Génétique, Reims, F-51092, France.
700    1_
$a Jennesson, Mélanie $u CHU Reims, American Memorial Hospital, Service de Pédiatrie, REIMS, F-51092, France.
700    1_
$a Sattar, Shifteh $u Department of Pediatric Neurology, Rady Children's Hospital/University of California, San Diego, California, USA.
700    1_
$a Marchal, Cécile $u Service d'Epileptologie Clinique, CHU de Bordeaux, France.
700    1_
$a Nordli, Douglas R $u Children's Hospital Los Angeles, Keck School of Medicine, University of Southern California, Los Angeles, California, USA.
700    1_
$a Lindstrom, Kristin $u Division of Genetics and Metabolism, Phoenix Children's Hospital, Phoenix, Arizona, USA.
700    1_
$a Striano, Pasquale $u Pediatric Neurology and Muscular Diseases Unit, Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, "G. Gaslini" Institute, Genova, Italy.
700    1_
$a Lomax, Lysa Boissé $u Department of Medicine, Divisions of Neurology and Respirology, Queen's University, Kingston, Ontario, Canada. Kingston Health Sciences Centre, Kingston, Ontario, K7L 2V7, Canada.
700    1_
$a Kiss, Courtney $u Kingston Health Sciences Centre, Kingston, Ontario, K7L 2V7, Canada.
700    1_
$a Bartolomei, Fabrice $u Pediatric Neurology Department, Timone Hospital, APHM, Marseille, France.
700    1_
$a Lepine, Anne Fabienne $u Pediatric Neurology Department, Timone Hospital, APHM, Marseille, France.
700    1_
$a Schoonjans, An-Sofie $u Department of Pediatric Neurology, Antwerp University Hospital, Edegem, Belgium.
700    1_
$a Stouffs, Katrien $u Vrije Universiteit Brussel (VUB), Universitair Ziekenhuis Brussel (UZ Brussel), Neurogenetics Research Group, Laarbeeklaan 101, 1090, Brussels, Belgium.
700    1_
$a Jansen, Anna $u Vrije Universiteit Brussel (VUB), Universitair Ziekenhuis Brussel (UZ Brussel), Neurogenetics Research Group, Laarbeeklaan 101, 1090, Brussels, Belgium.
700    1_
$a Panagiotakaki, Eleni $u Paediatric Clinical Epileptology, Sleep disorders and Functional Neurology, University Hospitals of Lyon (HCL), Lyon, France.
700    1_
$a Ricard-Mousnier, Brigitte $u Unité d'épileptologie, Service de Neurologie, CHU, 49033, Angers, France.
700    1_
$a Thevenon, Julien $u Inserm UMR 1231 GAD Team, Genetics of Developmental Anomalies, et FHU-TRANSLAD, CHU/Université de Bourgogne-Franche Comté, Dijon, France.
700    1_
$a de Bellescize, Julitta $u Paediatric Clinical Epileptology, Sleep disorders and Functional Neurology, University Hospitals of Lyon (HCL), Lyon, France.
700    1_
$a Catenoix, Hélène $u Paediatric Clinical Epileptology, Sleep disorders and Functional Neurology, University Hospitals of Lyon (HCL), Lyon, France.
700    1_
$a Dorn, Thomas $u Clinique Bernoise, Crans-, Montana, Switzerland.
700    1_
$a Zenker, Martin $u Institute of Human Genetics, University Hospital, Magdeburg, Germany.
700    1_
$a Müller-Schlüter, Karen $u Epilepsy Center for Children, Brandenburg Medical School, University Hospital, Neuruppin, Germany.
700    1_
$a Brandt, Christian $u Bethel Epilepsy Centre, Bielefeld, Germany.
700    1_
$a Krey, Ilona $u Institute of Human Genetics, University of Leipzig Hospitals and Clinics, Leipzig, Germany.
700    1_
$a Polster, Tilman $u Bethel Epilepsy Centre, Bielefeld, Germany.
700    1_
$a Wolff, Markus $u Department of Pediatric Neurology and Developmental Medicine, University Children's Hospital, Tübingen, Germany.
700    1_
$a Balci, Meral $u Department of Pediatric Neurology, Children's Hospital Datteln, Witten/Herdecke University, Datteln, Germany.
700    1_
$a Rostasy, Kevin $u Department of Pediatric Neurology, Children's Hospital Datteln, Witten/Herdecke University, Datteln, Germany.
700    1_
$a Achaz, Guillaume $u Institut de Systématique, Evolution, Biodiversité, ISYEB, UMR 7205 CNRS MNHN UPMC EPHE, Paris, France.
700    1_
$a Zacher, Pia $u The Saxon Epilepsy Center Kleinwachau, Radeberg, Germany.
700    1_
$a Becher, Thomas $u Kinderneurologisches Zentrum, Düsseldorf-Gerresheim, Sana Kliniken, Düsseldorf, Germany.
700    1_
$a Cloppenborg, Thomas $u Bethel Epilepsy Centre, Bielefeld, Germany.
700    1_
$a Yuskaitis, Christopher J $u Department of Neurology, F.M. Kirby Neurobiology Center, Boston Children's Hospital, Boston, Massachusetts, USA. Division of Epilepsy and Clinical Neurophysiology and Epilepsy Genetics Program, Boston Children's Hospital, Boston, Massachusetts, USA. Department of Neurology, Harvard Medical School, Boston, Massachusetts, USA.
700    1_
$a Weckhuysen, Sarah $u Neurogenetics Group, VIB-Department of Molecular Genetics, University of Antwerp, Antwerp, Belgium.
700    1_
$a Poduri, Annapurna $u Department of Neurology, F.M. Kirby Neurobiology Center, Boston Children's Hospital, Boston, Massachusetts, USA. Division of Epilepsy and Clinical Neurophysiology and Epilepsy Genetics Program, Boston Children's Hospital, Boston, Massachusetts, USA. Department of Neurology, Harvard Medical School, Boston, Massachusetts, USA.
700    1_
$a Lemke, Johannes R $u Institute of Human Genetics, University of Leipzig Hospitals and Clinics, Leipzig, Germany.
700    1_
$a Møller, Rikke S $u Danish Epilepsy Centre, Dianalund; Institute for Regional Health research, University of Southern Denmark, Odense, Denmark.
700    1_
$a Baulac, Stéphanie $u Sorbonne Université, UPMC Univ Paris 06, UMR S 1127, F-75013, Paris, France. stephanie.baulac@upmc.fr. INSERM, U1127, F-75013, Paris, France. stephanie.baulac@upmc.fr. CNRS, UMR 7225, F-75013, Paris, France. stephanie.baulac@upmc.fr. Institut du Cerveau et de la Moelle épinière (ICM), Hôpital Pitié-Salpêtrière, F-75013, Paris, France. stephanie.baulac@upmc.fr. Department of Genetics, Assistance Publique des Hôpitaux de Paris (AP-HP), Hôpital Pitié-Salpêtrière, F-75013, Paris, France. stephanie.baulac@upmc.fr.
773    0_
$w MED00186213 $t Genetics in medicine : official journal of the American College of Medical Genetics $x 1530-0366 $g Roč. 21, č. 2 (2019), s. 398-408
856    41
$u https://pubmed.ncbi.nlm.nih.gov/30093711 $y Pubmed
910    __
$a ABA008 $b sig $c sign $y a $z 0
990    __
$a 20190813 $b ABA008
991    __
$a 20190819113720 $b ABA008
999    __
$a ok $b bmc $g 1433428 $s 1066739
BAS    __
$a 3
BAS    __
$a PreBMC
BMC    __
$a 2019 $b 21 $c 2 $d 398-408 $e 20180810 $i 1530-0366 $m Genetics in medicine $n Genet Med $x MED00186213
GRA    __
$a 682345 $p European Research Council $2 International
GRA    __
$a K12 NS098482 $p NINDS NIH HHS $2 United States
LZP    __
$a Pubmed-20190813

Najít záznam

Citační ukazatele

Nahrávání dat ...

Možnosti archivace

Nahrávání dat ...