Dravet syndrome and its mimics: Beyond SCN1A
Author:
Affiliation:
1. The Paediatric Neurosciences Research Group; Royal Hospital for Children; Glasgow United Kingdom
2. School of Medicine; University of Glasgow; Glasgow United Kingdom
Funder
Epilepsy Research UK
Glasgow Children's Hospital Charity
Dravet Syndrome UK
Publisher
Wiley
Subject
Clinical Neurology,Neurology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/epi.13889/fullpdf
Reference75 articles.
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2. Spectrum of SCN1A gene mutations associated with Dravet syndrome: analysis of 333 patients;Depienne;J Med Genet,2009
3. Genotype-phenotype associations in SCN1A related epilepsies;Zuberi;Neurology,2011
4. Identification of an Na(v)1.1 sodium channel (SCN1A) loss-of-function mutation associated with familial simple febrile seizures;Mantegazza;Proc Natl Acad Sci USA,2005
5. Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+;Escayg;Nat Genet,2000
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