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SCN8A Mutation in Infantile Epileptic Encephalopathy: Report of Two Cases

Early infantile epileptic encephalopathy type 13 is a severe form of epilepsy caused by mutations in the sodium channel 8 alpha (SCN8A) gene. This gene encodes the neuronal voltage-gated sodium channel which plays vital role in neuronal excitability. Here we present two cases with SCN8A encephalopat...

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Detalles Bibliográficos
Autores principales:	Fatema, Kanij, Rahman, Md Mizanur, Faruk, Omar
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Korean Epilepsy Society 2019
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7251340/ https://www.ncbi.nlm.nih.gov/pubmed/32509551 http://dx.doi.org/10.14581/jer.19017

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