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...
| Other Authors: | , |
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| Format: | eBook |
| Language: | Inglés |
| Published: |
Cambridge :
Cambridge University Press
2022.
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| Edition: | First edition |
| Series: | Elements in genetics in epilepsy,
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| Subjects: | |
| See on Biblioteca Universitat Ramon Llull: | https://discovery.url.edu/permalink/34CSUC_URL/1im36ta/alma991009769410806719 |
Table of Contents:
- Patient, family and foundation perspectives
- Basic science of KCNQ2 and KCNQ3
- Genotype-phenotype correlations
- Treatment of KCNQ2-associated epilepsies.
