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Article

A novel PITX2c loss-of-function mutation associated with familial atrial fibrillation.

European journal of medical genetics - 1 Jan 2014

Wang Jun, Zhang Dai-Fu, Sun Yu-Min, Yang Yi-Qing

Abstract excerpt

Atrial fibrillation (AF) represents the most prevalent form of sustained cardiac arrhythmia and contributes substantially to cardiovascular morbidity and mortality. Aggregating evidence demonstrates that genetic risk factors play an important role in the pathogenesis of AF. However, AF is a genetically heterogeneous disease and the genetic defects responsible for AF in an overwhelming majority of patients remain...

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Share to Atrial Fibrillation
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Homeobox Protein PITX2

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Source

Identifiers

PMID: 24333117
DOI: 10.1016/j.ejmg.2013.11.004

Provenance

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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