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Article

Tandem pore domain K(+)-channel TASK-3 (KCNK9) and idiopathic absence epilepsies.

American journal of medical genetics - 8 Mar 2002

Kananura Colette, Sander Thomas, Rajan Sindhu, Preisig-Müller Regina, Grzeschik Karl-Heinz, Daut Jürgen, Derst Christian, Steinlein Ortrud K

Abstract excerpt

Recently, the gene coding for the tandem pore domain K(+)-channel TASK-3 (KCNK9) has been localized to the chromosomal region 8q24. Because mutations in ion channel genes have been recognized as an important factor in the etiology of abnormal neuronal excitability, TASK-3 is an interesting candidate gene for epilepsies linked to 8q24. We therefore performed a mutation analysis of the TASK-3 gene in 65 patients...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Polymorphism, Single-Stranded Conformational

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Source

Identifiers

PMID: 11857586
DOI: 10.1002/ajmg.10201

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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Tandem pore domain K(+)-channel TASK-3 (KCNK9) and idiopathic absence epilepsies.PMID 11857586Read ↗

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