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Article

A novel PITX2c loss‑of‑function mutation underlies lone atrial fibrillation.

International journal of molecular medicine - 1 Oct 2013

Zhou Yi-Meng, Zheng Peng-Xiang, Yang Yi-Qing, Ge Zhi-Ming, Kang Wei-Qiang

Abstract excerpt

Atrial fibrillation (AF) is the most common form of sustained cardiac arrhythmia responsible for substantial morbidity and significantly increased mortality rates. A growing body of evidence documents the important role of genetic defects in the pathogenesis of AF. However, AF is a heterogeneous disease and the genetic determinants for AF in an overwhelming majority of patients remain unknown. In the present...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 23913021
DOI: 10.3892/ijmm.2013.1463

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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