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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Dettagli Bibliografici
Pubblicato in:Neurobiol Dis
Autori principali: Lamar, Tyra, Vanoye, Carlos G., Calhoun, Jeffrey, Wong, Jennifer C., Dutton, Stacey B.B., Jorge, Benjamin S., Velinov, Milen, Escayg, Andrew, Kearney, Jennifer A.
Natura: Artigo
Lingua:Inglês
Pubblicazione: 2017
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Article
Accesso online: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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