A Common Kinetic Property of Mutations Linked to Episodic Ataxia Type 1 Studied in the Shaker Kv Channel

(1) Background: Episodic ataxia type 1 is caused by mutations in the KCNA1 gene encoding for the voltage-gated potassium channel Kv1.1. There have been many mutations in Kv1.1 linked to episodic ataxia reported and typically investigated by themselves or in small groups. The aim of this article is t...

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Detalles Bibliográficos
Autores principales: Zhao, Juan, Petitjean, Dimitri, Haddad, Georges A., Batulan, Zarah, Blunck, Rikard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7589002/
https://www.ncbi.nlm.nih.gov/pubmed/33066705
http://dx.doi.org/10.3390/ijms21207602

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7589002/
https://www.ncbi.nlm.nih.gov/pubmed/33066705
http://dx.doi.org/10.3390/ijms21207602

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