Neuronal Nicotinic Acetylcholine Receptors and Epilepsy
The identification of a genetically transmissible form of epilepsy that is associated with a mutation in CHRNA4, the gene that encodes the α4 subunit of the high-affinity nicotinic acetylcholine receptor, was the first demonstration that an alteration in a ligand-gated ion channel can cause seizures...
Guardado en:
| Publicado en: | Epilepsy Curr |
|---|---|
| Autor principal: | |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
American Epilepsy Society
2002
|
| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC321143/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/15309115/ https://ncbi.nlm.nih.govhttps://doi.org/10.1046/j.1535-7597.2002.00072.x |
| Etiquetas: |
Sin Etiquetas, Sea el primero en etiquetar este registro!
|