KCNQ2- and KCNQ3-associated epilepsy
KCNQ2 and KCNQ3 encode subunits (KV7.2, KV7.3) that combine to form a voltage-gated potassium ion (K+) channel responsible for generating an ionic current (M-current) important for controlling activity in the nervous system. Pathogenic variants in both genes are associated with a spectrum of genetic...
| Otros Autores: | , |
|---|---|
| Formato: | Libro electrónico |
| Idioma: | Inglés |
| Publicado: |
Cambridge :
Cambridge University Press
2022.
|
| Edición: | First edition |
| Colección: | Elements in genetics in epilepsy,
|
| Materias: | |
| Ver en Biblioteca Universitat Ramon Llull: | https://discovery.url.edu/permalink/34CSUC_URL/1im36ta/alma991009769410806719 |
Tabla de Contenidos:
- Patient, family and foundation perspectives
- Basic science of KCNQ2 and KCNQ3
- Genotype-phenotype correlations
- Treatment of KCNQ2-associated epilepsies.
