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Article

Arrhythmogenic cardiomyopathy in a patient with a rare loss-of-function KCNQ1 mutation.

Journal of the American Heart Association - 23 Jan 2015

Xiong Qinmei, Cao Qing, Zhou Qiongqiong, Xie Jinyan, Shen Yang, Wan Rong, Yu Jianhua, Yan Sujuan, Marian Ali J, Hong Kui

Abstract excerpt

BACKGROUND: Ventricular tachycardia (VT) is a common manifestation of advanced cardiomyopathies. In a subset of patients with dilated cardiomyopathy, VT is the initial and the cardinal manifestation of the disease. The molecular genetic basis of this subset of dilated cardiomyopathy is largely unknown. METHODS AND RESULTS: We identified 10 patients with dilated cardiomyopathy who presented with VT and sequenced...

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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: 25616976
DOI: 10.1161/JAHA.114.001526
PMCID: PMC4330077

Genes

KCNQ1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

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