Convulsive seizures and SUDEP in a mouse model of SCN8A epileptic encephalopathy

De novo mutations of the voltage-gated sodium channel gene SCN8A have recently been recognized as a cause of epileptic encephalopathy, which is characterized by refractory seizures with developmental delay and cognitive disability. We previously described the heterozygous SCN8A missense mutation p.A...

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Detalles Bibliográficos
Autores principales: Wagnon, Jacy L., Korn, Matthew J., Parent, Rachel, Tarpey, Taylor A., Jones, Julie M., Hammer, Michael F., Murphy, Geoffrey G., Parent, Jack M., Meisler, Miriam H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2015
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4275076/
https://www.ncbi.nlm.nih.gov/pubmed/25227913
http://dx.doi.org/10.1093/hmg/ddu470

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4275076/
https://www.ncbi.nlm.nih.gov/pubmed/25227913
http://dx.doi.org/10.1093/hmg/ddu470

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