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Correction: Consensus statement on standards and guidelines for the molecular diagnostics of Alport syndrome: refining the ACMG criteria

Savige, Judy
Autor Savige, Judy ORCID Department of Medicine (MH and NH), The University of Melbourne, Parkville, VIC, Australia. jasavige@unimelb.edu.au
Storey, Helen
Autor Storey, Helen ORCID Molecular Genetics, Viapath Laboratories, Guy's Hospital, London, UK
Watson, Elizabeth
Autor Watson, Elizabeth Elizabeth Watson, South West Genomic Laboratory Hub, North Bristol Trust, Bristol, UK
Hertz, Jens Michael
Autor Hertz, Jens Michael Jens Michael Hertz, Department of Clinical Genetics, Odense University Hospital, Odense, Denmark
Deltas, Constantinos
Autor Deltas, Constantinos ORCID Center of Excellence in Biobanking and Biomedical Research and Molecule Medicine Center, University of Cyprus, Nicosia, Cyprus
Renieri, Alessandra
Autor Renieri, Alessandra ORCID Medical Genetics, University of Siena, Siena, Italy
Mari, Francesca
Autor Mari, Francesca Institute de Pathologie et de Genetique ASBL, Departement de Biologie Moleculaire, Gosselies, Belgium
Hilbert, Pascale
Autor Hilbert, Pascale ORCID Institute de Pathologie et de Genetique ASBL, Departement de Biologie Moleculaire, Gosselies, Belgium
Plevova, Pavlina
Autor Plevova, Pavlina Department of Medical Genetics, and Department of Biomedical Sciences, University Hospital of Ostrava, Ostrava, Czech Republic
Byers, Peter
Autor Byers, Peter Departments of Pathology and Medicine (Medical Genetics), University of Washington, Seattle, WA, USA
Cerkauskaite, Agne
Autor Cerkauskaite, Agne Institute of Biomedical Sciences, Faculty of Medicine, Vilnius University, Vilnius, Lithuania
Gregory, Martin
Autor Gregory, Martin Division of Nephrology, Department of Medicine, University of Utah Health, Salt Lake City, UT, USA
Cerkauskiene, Rimante
Autor Cerkauskiene, Rimante Clinic of Pediatrics, Institute of Clinical Medicine, Faculty of Medicine, Vilnius University, Vilnius, Lithuania
Ljubanovic, Danica Galesic
Autor Ljubanovic, Danica Galesic Department of Pathology, University of Zagreb, School of Medicine, Dubrava University Hospital, Zagreb, Croatia
Becherucci, Francesca
Autor Becherucci, Francesca Nephrology Unit and Meyer Children's University Hospital, Firenze, Italy
Errichiello, Carmela
Autor Errichiello, Carmela Nephrology Unit and Meyer Children's University Hospital, Firenze, Italy
Massella, Laura
Autor Massella, Laura Division of Nephrology and Dialysis, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy
Aiello, Valeria
Autor Aiello, Valeria Department of Experimental Diagnostic and Specialty Medicine (DIMES), Nephrology, Dialysis and Renal Transplant Unit, S. Orsola Hospital, University of Bologna, Bologna, Italy
Lennon, Rachel
Autor Lennon, Rachel Wellcome Centre for Cell-Matrix Research, Division of Cell-Matrix Biology and Regenerative Medicine, School of Biological Sciences, Faculty of Biology Medicine and Health, The University of Manchester, Manchester, UK
Hopkinson, Louise
Autor Hopkinson, Louise ORCID Wellcome Centre for Cell-Matrix Research, Division of Cell-Matrix Biology and Regenerative Medicine, School of Biological Sciences, Faculty of Biology Medicine and Health, The University of Manchester, Manchester, UK
Koziell, Ania
Autor Koziell, Ania School of Immunology and Microbial Sciences, Faculty of Life Sciences, King's College London, London, UK
Lungu, Adrian
Autor Lungu, Adrian Fundeni Clinical Institute, Pediatric Nephrology Department, Bucharest, Romania
Rothe, Hansjorg Martin
Autor Rothe, Hansjorg Martin ORCID Centre for Nephrology and Metabolic Disorders, Weisswasser, Germany
Hoefele, Julia
Autor Hoefele, Julia ORCID Institute of Human Genetics, Technical University of Munich, München, Germany
Zacchia, Miriam
Autor Zacchia, Miriam Nephrology Unit, University of Campania, Naples, Italy
Martic, Tamara Nikuseva
Autor Martic, Tamara Nikuseva Department of Biology, School of Medicine University of Zagreb, Zagreb, Croatia
Gupta, Asheeta
Autor Gupta, Asheeta Birmingham Children's Hospital, Birmingham, UK
van Eerde, Albertien
Autor van Eerde, Albertien Departments of Genetics and Center for Molecular Medicine, University Medical Center, Utrecht University, Utrecht, The Netherlands
Gear, Susie
Autor Gear, Susie Alport UK, Gloucester, UK
Landini, Samuela
Autor Landini, Samuela ORCID Medical Genetics Unit, Department of Clinical and Experimental Biomedical Sciences "Mario Serio", University of Florence, Florence, Italy
Palazzo, Viviana
Autor Palazzo, Viviana Medical Genetics Unit, Meyer Children's University Hospital, Florence, Italy
Al-Rabadi, Laith
Autor Al-Rabadi, Laith Health Sciences Centre, University of UTAH, Salt Lake City, UT, USA
Claes, Kathleen
Autor Claes, Kathleen ORCID Department of Nephrology and Renal Transplantation, University Hospitals Leuven, Leuven, Belgium
Corveleyn, Anniek
Autor Corveleyn, Anniek Center for Human Genetics, University Hospitals and KU Leuven, Leuven, Belgium
Van Hoof, Evelien
Autor Van Hoof, Evelien Center for Human Genetics, University Hospitals and KU Leuven, Leuven, Belgium
van Geel, Micheel
Autor van Geel, Micheel Department of Clinical Genetics, Maastricht University Medical Center, Maastricht, The Netherlands
Williams, Maggie
Autor Williams, Maggie Bristol Genetics Laboratory Pathology Sciences, Southmead Hospital, Bristol, UK
Ashton, Emma
Autor Ashton, Emma North East Thames Regional Genetics Laboratory, Great Ormond Street Hospital, London, UK
Belge, Hendica
Autor Belge, Hendica Department of Physiology, Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, Nijmegen, The Netherlands
Ars, Elisabeth
Autor Ars, Elisabeth Inherited Kidney Disorders, Fundacio Puigvert, Universitat Autonoma de Barcelona, Barcelona, Spain
Bierzynska, Agnieszka
Autor Bierzynska, Agnieszka Bristol Renal Unit, Bristol Medical School, University of Bristol, Bristol, UK
Gangemi, Concetta
Autor Gangemi, Concetta Division of Nephrology and Dialysis, University Hospital of Verona, Verona, Italy
Lipska-Ziętkiewicz, Beata S
Autor Lipska-Ziętkiewicz, Beata S Centre for Rare Diseases, and Clinical Genetics Unit, Medical University of Gdansk, Gdansk, Poland

European journal of human genetics. 2024 Jan ; 32 (1) : 132.

Eur J Hum Genet
ISSN 1476-5438 | 1018-4813
Zdroj

Status PubMed-not-MEDLINE Jazyk angličtina Země Velká Británie, Anglie Médium print

Typ dokumentu tisková chyba

Perzistentní odkaz https://www.medvik.cz/link/pmid36721056

Online Plný text

PubMed 36721056
PubMed Central PMC10772080
DOI 10.1038/s41431-023-01288-x
PII: 10.1038/s41431-023-01288-x
Knihovny.cz E-zdroje

Publikační typ
tisková chyba MeSH

Alport UK Gloucester UK

Birmingham Children's Hospital Birmingham UK

Bristol Genetics Laboratory Pathology Sciences Southmead Hospital Bristol UK

Bristol Renal Unit Bristol Medical School University of Bristol Bristol UK

Center for Human Genetics University Hospitals and KU Leuven Leuven Belgium

Center of Excellence in Biobanking and Biomedical Research and Molecule Medicine Center University of Cyprus Nicosia Cyprus

Centre for Nephrology and Metabolic Disorders Weisswasser Germany

Centre for Rare Diseases and Clinical Genetics Unit Medical University of Gdansk Gdansk Poland

Clinic of Pediatrics Institute of Clinical Medicine Faculty of Medicine Vilnius University Vilnius Lithuania

Department of Biology School of Medicine University of Zagreb Zagreb Croatia

Department of Clinical Genetics Maastricht University Medical Center Maastricht The Netherlands

Department of Experimental Diagnostic and Specialty Medicine Nephrology Dialysis and Renal Transplant Unit S Orsola Hospital University of Bologna Bologna Italy

Department of Medical Genetics and Department of Biomedical Sciences University Hospital of Ostrava Ostrava Czech Republic

Department of Medicine The University of Melbourne Parkville VIC Australia

Department of Nephrology and Renal Transplantation University Hospitals Leuven Leuven Belgium

Department of Pathology University of Zagreb School of Medicine Dubrava University Hospital Zagreb Croatia

Department of Physiology Radboud Institute for Molecular Life Sciences Radboud University Medical Center Nijmegen The Netherlands

Departments of Genetics and Center for Molecular Medicine University Medical Center Utrecht University Utrecht The Netherlands

Departments of Pathology and Medicine University of Washington Seattle WA USA

Division of Nephrology and Dialysis Bambino Gesù Children's Hospital IRCCS Rome Italy

Division of Nephrology and Dialysis University Hospital of Verona Verona Italy

Division of Nephrology Department of Medicine University of Utah Health Salt Lake City UT USA

Elizabeth Watson South West Genomic Laboratory Hub North Bristol Trust Bristol UK

Fundeni Clinical Institute Pediatric Nephrology Department Bucharest Romania

Health Sciences Centre University of UTAH Salt Lake City UT USA

Inherited Kidney Disorders Fundacio Puigvert Universitat Autonoma de Barcelona Barcelona Spain

Institute de Pathologie et de Genetique ASBL Departement de Biologie Moleculaire Gosselies Belgium

Institute of Biomedical Sciences Faculty of Medicine Vilnius University Vilnius Lithuania

Institute of Human Genetics Technical University of Munich München Germany

Jens Michael Hertz Department of Clinical Genetics Odense University Hospital Odense Denmark

Medical Genetics Unit Department of Clinical and Experimental Biomedical Sciences Mario Serio University of Florence Florence Italy

Medical Genetics Unit Meyer Children's University Hospital Florence Italy

Medical Genetics University of Siena Siena Italy

Molecular Genetics Viapath Laboratories Guy's Hospital London UK

Nephrology Unit and Meyer Children's University Hospital Firenze Italy

Nephrology Unit University of Campania Naples Italy

North East Thames Regional Genetics Laboratory Great Ormond Street Hospital London UK

School of Immunology and Microbial Sciences Faculty of Life Sciences King's College London London UK

Wellcome Centre for Cell Matrix Research Division of Cell Matrix Biology and Regenerative Medicine School of Biological Sciences Faculty of Biology Medicine and Health The University of Manchester Manchester UK

Erratum pro

Eur J Hum Genet. 2021 Aug;29(8):1186-1197. doi: 10.1038/s41431-021-00858-1. PubMed

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Correction: Consensus statement on standards and guidelines for the molecular diagnostics of Alport syndrome: refining the ACMG criteria

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