reference/14079881

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publicationName	Epilepsy Research
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bibliographicCitation	Wang JW, Shi XY, Kurahashi H, Hwang SK, Ishii A, Higurashi N, Kaneko S, Hirose S; Epilepsy Genetic Study Group Japan. Prevalence of SCN1A mutations in children with suspected Dravet syndrome and intractable childhood epilepsy. Epilepsy Res. 2012 Dec;102(3):195–200. doi: 10.1016/j.eplepsyres.2012.06.006. PMID: 23195492.
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identifier	https://pubmed.ncbi.nlm.nih.gov/23195492 https://doi.org/10.1016/j.eplepsyres.2012.06.006
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	Prevalence of SCN1A mutations in children with suspected Dravet syndrome and intractable childhood epilepsy
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