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Article

Mutation in the S3 segment of KCNQ1 results in familial lone atrial fibrillation.

Heart rhythm - 1 Aug 2009

Das Saumya, Makino Seiko, Melman Yonathan F, Shea Marisa A, Goyal Sanjeev B, Rosenzweig Anthony, Macrae Calum A, Ellinor Patrick T

Abstract excerpt

BACKGROUND: Mutations in several ion channel genes have been reported to cause rare cases of familial atrial fibrillation (AF). OBJECTIVE: The purpose of this study was to determine the genetic basis for AF in a family with autosomal dominant AF. METHODS: Family members were evaluated by 12-lead...

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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: 19632626
DOI: 10.1016/j.hrthm.2009.04.015
PMCID: PMC3038671

Genes

KCNQ1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-19632626-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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