Hereditary Channelopathies in Neurology

Erstveröffentlichung
2010
Authors
Jurkat-Rott, Karin
Lerche, Holger
Weber, Yvonne
Lehmann-Horn, Frank
Teil eines Buches


Published in
Rare Diseases Epidemiology / DelaPaz, MP ; Groft, SC (Hrsg.). - Berlin : Springer Verlag, 2010. - (Advances in Experimental Medicine and Biology ; 686). - S. 305-334. - ISBN 978-90-481-9484-1. - ISSN 0065-2598
Link to publication
https://dx.doi.org/10.1007/978-90-481-9485-8_18
Faculties
Medizinische Fakultät
Institutions
Institut für Angewandte Physiologie
Subject headings
[Free subject headings]: Epilepsy | Ataxia | Migraine | Pain | Neuromyotonia | Myasthenia | Myotonia | Periodic-paralysis | familial hemiplegic migraine | hypokalemic periodic paralysis | severe myoclonic epilepsy | sodium-channel mutations | idiopathic generalized epilepsy | extreme pain disorder | de-novo mutations | dominant cerebellar-ataxia | childhood absence epilepsy | of-function mutations
[DDC subject group]: DDC 610 / Medicine & health
Metadata
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