Temperature- and age-dependent seizures in a mouse model of severe myoclonic epilepsy in infancy

Heterozygous loss-of-function mutations in the α subunit of the type I voltage-gated sodium channel Na(V)1.1 cause severe myoclonic epilepsy in infancy (SMEI), an infantile-onset epileptic encephalopathy characterized by normal development followed by treatment-refractory febrile and afebrile seizur...

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Detaylı Bibliyografya
Asıl Yazarlar: Oakley, John C., Kalume, Franck, Yu, Frank H., Scheuer, Todd, Catterall, William A.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: National Academy of Sciences 2009
Konular:
Biological Sciences
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC2656193/
https://ncbi.nlm.nih.gov/pubmed/19234123
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0813330106
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