학술논문
Whole exome sequencing identifies a novel SCN1A mutation in genetic (idiopathic) generalized epilepsy and juvenile myoclonic epilepsy subtypes.
Document Type
Journal Article
Author
Source
Subject
*CALMODULIN
*EPILEPSY
*FEBRILE seizures
*SODIUM channels
*ETIOLOGY of diseases
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Language
ISSN
1590-1874
Abstract