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Article

Identification of a KCNE2 Gain-of-Function Mutation in Patients with Familial Atrial Fibrillation

4 Oct 2004

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Share to Cardiac Arrhythmias and Treatments
Share to Cardiac electrophysiology and arrhythmias
Share to Ion channel regulation and function

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 15368194
DOI: 10.1086/425342

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

Identification of a KCNE2 Gain-of-Function Mutation in Patients with Familial Atrial FibrillationPMID 15368194Read ↗

Gain-of-function mutations in potassium channel subunit KCNE2 associated with early-onset lone atrial fibrillation.Semantic proximity Read ↗

Progressive myoclonus epilepsy caused by a gain-of-function KCNA2 mutationSemantic proximity Read ↗

A gain of function mutation in PITX2c gene linked to atrial fibrillation alters mitochondrial function and membrane excitability.Semantic proximity Read ↗

Novel KCNA5 loss-of-function mutations responsible for atrial fibrillation.Semantic proximity Read ↗

Loss-of-function mutations of the K+ channel gene KCNJ2 constitute a rare cause of long QT syndromeSemantic proximity Read ↗

[KCNE3 R53H substitution in familial atrial fibrillation].Semantic proximity Read ↗

Functional characterization of a novel mutation in KCNA1 in episodic ataxia type 1 associated with epilepsy.Semantic proximity Read ↗

High-throughput functional mapping of variants in an arrhythmia gene, KCNE1, reveals novel biology.Semantic proximity Read ↗

Characterisation of the human voltage-gated potassium channel gene, KCNA7, a candidate gene for inherited cardiac disorders, and its exclusion as cause of progressive familial heart block I (PFHBI)Semantic proximity Read ↗

A Novel Loss-of-Function Variant in the Chloride Ion Channel Gene Clcn2 Associates with Atrial Fibrillation.Semantic proximity Read ↗

A novel KCND3 gain-of-function mutation associated with early-onset of persistent lone atrial fibrillation.Semantic proximity Read ↗

A Novel KCNA2 Variant in a Patient with Non-Progressive Congenital Ataxia and Epilepsy: Functional Characterization and Sensitivity to 4-AminopyridineSemantic proximity Read ↗

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