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Article

Kv7.1 (KCNQ1) properties and channelopathies.

The Journal of physiology - 1 Apr 2008

Peroz David, Rodriguez Nicolas, Choveau Frank, Baró Isabelle, Mérot Jean, Loussouarn Gildas

Abstract excerpt

KCNQ1 is the pore-forming subunit of a channel complex whose expression and function have been rather well characterized in the heart. Almost 300 mutations of KCNQ1 have been identified in patients and a vast majority of the described mutations are linked to the long QT syndrome. Only a few mutations are linked to other pathologies such as atrial fibrillation and the short QT syndrome. However, a considerable...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 18174212
DOI: 10.1113/jphysiol.2007.148254
PMCID: PMC2375722

Genes

KCNQ1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

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