SCN3A deficiency associated with increased seizure susceptibility

Mutations in voltage-gated sodium channels expressed highly in the brain (SCN1A, SCN2A, SCN3A, and SCN8A) are responsible for an increasing number of epilepsy syndromes. In particular, mutations in the SCN3A gene, encoding the pore-forming Na(v)1.3 α subunit, have been identified in patients with fo...

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Detalhes bibliográficos
Publicado no:Neurobiol Dis
Main Authors: Lamar, Tyra, Vanoye, Carlos G., Calhoun, Jeffrey, Wong, Jennifer C., Dutton, Stacey B.B., Jorge, Benjamin S., Velinov, Milen, Escayg, Andrew, Kearney, Jennifer A.
Formato: Artigo
Idioma:Inglês
Publicado em: 2017
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5446790/
https://ncbi.nlm.nih.gov/pubmed/28235671
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.nbd.2017.02.006
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