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Severe paroxysmal dyskinesias without epilepsy in a RHOBTB2 mutation carrier

J. Necpál, M. Zech, A. Valachová, Z. Sedláček, Š. Bendová, M. Hančárová, K. Okáľová, J. Winkelmann, R. Jech

. 2020 ; 77 (-) : 87-88. [pub] 20200629

Language English Country Great Britain

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

Persistent link   https://www.medvik.cz/link/bmc21026636

Grant support
NV17-29423A MZ0 CEP Register

References provided by Crossref.org

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$a Zech, Michael $u Institute of Neurogenomics, Helmholtz Zentrum München, Munich, Germany; Institute of Human Genetics, Technical University of Munich, Munich, Germany
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$a Valachová, Alica $u Department of Clinical Genetics, Faculty Hospital Trenčín, Trenčín, Slovakia
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$a Sedláček, Zdeněk $u Department of Biology and Medical Genetics, Charles University 2nd Faculty of Medicine and University Hospital Motol, Prague, Czech Republic
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$a Bendová, Šárka $u Department of Biology and Medical Genetics, Charles University 2nd Faculty of Medicine and University Hospital Motol, Prague, Czech Republic
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$a Hančárová, Miroslava $u Department of Biology and Medical Genetics, Charles University 2nd Faculty of Medicine and University Hospital Motol, Prague, Czech Republic
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$a Okáľová, Katarína $u 2nd Pediatric Clinic, Slovak Medical University, Banská Bystrica, Slovakia
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$a Winkelmann, Juliane $u Institute of Neurogenomics, Helmholtz Zentrum München, Munich, Germany; Institute of Human Genetics, Technical University of Munich, Munich, Germany; Lehrstuhl für Neurogenetik, Technische Universität München, Munich, Germany; Munich Cluster for Systems Neurology, SyNergy, Munich, Germany
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$a 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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