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Article

A novel PRKAG2 mutation in a Chinese family with cardiac hypertrophy and ventricular pre-excitation.

Scientific reports - 25 May 2017

Yang Kun-Qi, Lu Chao-Xia, Zhang Ying, Yang Yan-Kun, Li Jia-Cheng, Lan Tian, Meng Xu, Fan Peng, Tian Tao, Wang Lin-Ping, Liu Ya-Xin, Zhang Xue, Zhou Xian-Liang

Abstract excerpt

PRKAG2 syndrome is a rare autosomal dominant inherited disorder that is characterized by cardiac hypertrophy, ventricular pre-excitation and conduction system abnormalities. There is little knowledge in cardiovascular magnetic resonance (CMR) characteristics of PRKAG2 cardiomyopathy. This study investigated the genetic defect in a three-generation Chinese family with cardiac hypertrophy and ventricular...

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Source

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Identifiers

PMID: 28546535
DOI: 10.1038/s41598-017-02455-z
PMCID: PMC5445094

Genes

PRKAG2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

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