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Article

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

International journal of molecular sciences - 14 Oct 2020

Zhao Juan, Petitjean Dimitri, Haddad Georges A, Batulan Zarah, Blunck Rikard

Abstract excerpt

(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 to determine whether we can define a functional parameter common to all Kv1.1 mutants that have been linked to...

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Identifiers

PMID: 33066705
DOI: 10.3390/ijms21207602
PMCID: PMC7589002

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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