Dravet syndrome-From epileptic encephalopathy to channelopathy
Author:
Affiliation:
1. The Paediatric Neurosciences Research Group; Royal Hospital for Sick Children; Glasgow United Kingdom
2. College of Medicine, Veterinary & Life Sciences; University of Glasgow; Glasgow United Kingdom
Funder
Muir Maxwell Trust
Epilepsy Research UK
Dravet Syndrome UK
Publisher
Wiley
Subject
Neurology (clinical),Neurology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/epi.12652/fullpdf
Reference47 articles.
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2. Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2;Escayg;Nat Genet,2000
3. The spectrum of SCN1A-related infantile epileptic encephalopathies;Harkin;Brain,2007
4. Generalized epilepsy with febrile seizures plus. A genetic disorder with heterogeneous clinical phenotypes;Scheffer;Brain,1997
5. Genotype-phenotype associations in SCN1A related epilepsies;Zuberi;Neurology,2011
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