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Article

A TASK3 channel (KCNK9) mutation in a genetic model of absence epilepsy.

Journal of molecular neuroscience : MN - 1 Jan 2005

Holter Jethro, Carter David, Leresche Nathalie, Crunelli Vincenzo, Vincent Pierre

Abstract excerpt

Childhood absence epilepsy is an idiopathic, generalized, nonconvulsive epilepsy with a multifactorial genetic etiology. The KCNK9 gene coding for the TASK3 (Twik-like acid-sensitive K</U)+) channel is present on chromosome 8 at position 8q24, a locus that has shown positive linkage to the human absence epilepsy phenotype. Sequencing of the KCNK9 gene in the genetic absence epilepsy rats from Strasbourg (GAERS),...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 15781965
DOI: 10.1385/JMN:25:1:037

Genes

KCNK9

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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