SCN1A channelopathies: Navigating from genotype to neural circuit dysfunction
The SCN1A gene is strongly associated with epilepsy and plays a central role for supporting cortical excitation-inhibition balance through the expression of NaV1.1 within inhibitory interneurons. The phenotype of SCN1A disorders has been conceptualized as driven primarily by impaired interneuron fun...
Na minha lista:
| Principais autores: | , |
|---|---|
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Frontiers Media S.A.
2023-04-01
|
| Colecção: | Frontiers in Neurology |
| Assuntos: | |
| Acesso em linha: | https://www.frontiersin.org/articles/10.3389/fneur.2023.1173460/full |
| Tags: |
Sem tags, seja o primeiro a adicionar uma tag!
|