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A de novo GRIA3 variant with complex hyperkinetic movement disorder in a girl with developmental delay and self-limited epilepsy

J. Necpál, J. Winkelmann, M. Zech, R. Jech

. 2023 ; 111 (-) : 105437. [pub] 20230505

Language English Country England, Great Britain

Document type Letter, Research Support, Non-U.S. Gov't

Persistent link   https://www.medvik.cz/link/bmc23011176

References provided by Crossref.org

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$a Necpál, Ján $u 2nd Department of Neurology, Faculty of Medicine, Comenius University, Bratislava, Slovakia; Department of Neurology, Zvolen Hospital, Zvolen, Slovakia. Electronic address: necpal.neuro@gmail.com
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$a A de novo GRIA3 variant with complex hyperkinetic movement disorder in a girl with developmental delay and self-limited epilepsy / $c J. Necpál, J. Winkelmann, M. Zech, R. Jech
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$a Winkelmann, Juliane $u Institute of Neurogenomics, Helmholtz Zentrum München, Munich, Germany; Institute of Human Genetics, School of Medicine, Technical University of Munich, Munich, Germany; Lehrstuhl für Neurogenetik, Technische Universität München, Munich, Germany; Munich Cluster for Systems Neurology, SyNergy, Munich, Germany
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$a Zech, Michael $u Institute of Neurogenomics, Helmholtz Zentrum München, Munich, Germany; Institute of Human Genetics, School of Medicine, Technical University of Munich, Munich, Germany
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$a Jech, Robert $u Department of Neurology and Center of Clinical Neuroscience, First Faculty of Medicine, Charles University and General University Hospital in Prague, Prague, Czech Republic
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$w MED00006198 $t Parkinsonism & related disorders $x 1873-5126 $g Roč. 111, č. - (2023), s. 105437
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