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Article

The KVLQT1 gene is not a common target for mutations in patients with various heart pathologies.

Journal of applied genetics - 1 Jan 2002

Moric Ewa, Herbert Ernest, Mazurek Urszula, Samelska Justyna, Cholewa Krzysztof, Trusz-Gluza Maria, Wilczok Tadeusz

Abstract excerpt

The long QT syndrome (LQTS) is a disorder of ventricular repolarization that exposes affected individuals to cardiac arrhythmias and sudden death. The first gene for LQTS has been mapped to chromosome 11 p.15.5 by genome-wide linkage analysis. This gene, originally named KVLQT1 (and later KCNQ1), is a novel potassium channel gene. Mutations in the human KVLQT1 gene, encoding the alpha-subunit of the KVLQT1...

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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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Share to Potassium Channels, Voltage-Gated

Share to Sequence Analysis, DNA

Source

Identifiers

PMID: 12080180

Genes

KCNQ1

Provenance

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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