Carregando...
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...
Na minha lista:
| Publicado no: | Neurobiol Dis |
|---|---|
| Principais autores: | , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2017
|
| Assuntos: | |
| 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 |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|