Mutation of sodium channel SCN3A in a patient with cryptogenic pediatric partial epilepsy

Mutations in the sodium channel genes SCN1A and SCN2A have been identified in monogenic childhood epilepsies, but SCN3A has not previously been investigated as a candidate gene for epilepsy. We screened a consecutive cohort of 18 children with cryptogenic partial epilepsy that was classified as phar...

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Detaylı Bibliyografya
Asıl Yazarlar: Holland, Katherine D., Kearney, Jennifer A., Glauser, Tracy A., Buck, Gerri, Keddache, Mehdi, Blankston, John, Glaaser, Ian, Kass., Robert S., Meisler, Miriam H
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2008
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Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC2423278/
https://ncbi.nlm.nih.gov/pubmed/18242854
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.neulet.2007.12.064
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