A homozygous mutation of voltage-gated sodium channel βIgeneSCN1Bin a patient with Dravet syndrome
Author:
Publisher
Wiley
Subject
Neurology (clinical),Neurology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/epi.12040/fullpdf
Reference14 articles.
1. Na+ channel β subunits: overachievers of the ion channel family;Brackenbury;Front Pharmacol,2011
2. De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy;Claes;Am J Hum Genet,2001
3. A proposed diagnostic scheme for people with epileptic seizures and with epilepsy: report of the ILAE Task Force on Classification and Terminology;Engel;Epilepsia,2001
4. Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2;Escayg;Nat Genet,2000
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