A carregar...
An Scn1a epilepsy mutation in Scn8a alters seizure susceptibility and behavior
Understanding the role of SCN8A in epilepsy and behavior is critical in light of recently identified human SCN8A epilepsy mutations. We have previously demonstrated that Scn8a(med) and Scn8a(med-jo) mice carrying mutations in the Scn8a gene display increased resistance to flurothyl and kainic acid-i...
Na minha lista:
| Publicado no: | Exp Neurol |
|---|---|
| Main Authors: | , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2015
|
| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4688066/ https://ncbi.nlm.nih.gov/pubmed/26410685 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.expneurol.2015.09.008 |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|