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Article

KCNE3 mutation V17M identified in a patient with lone atrial fibrillation.

Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology - 1 Jan 2008

Lundby Alicia, Ravn Lasse Steen, Svendsen Jesper Hastrup, Hauns Stig, Olesen Søren-Peter, Schmitt Nicole

Abstract excerpt

BACKGROUND: Atrial fibrillation (AF) is the most common cardiac rhythm disorder with a lifetime risk for development of 25% for people aged 40 or older. In this study we aim for the functional assessment of a mutation in KCNE3 identified in a proband with early-onset lone AF. METHODS: Screening of genomic DNA from the proband led to identification of a KCNE3 V17M missense mutation. We heterologously expressed the...

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Identifiers

PMID: 18209471
DOI: 10.1159/000113746

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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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