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

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

Abstract 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 s...

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Bibliographic Details
Main Authors: Kun-Qi Yang, Chao-Xia Lu, Ying Zhang, Yan-Kun Yang, Jia-Cheng Li, Tian Lan, Xu Meng, Peng Fan, Tao Tian, Lin-Ping Wang, Ya-Xin Liu, Xue Zhang, Xian-Liang Zhou
Format: Article
Language:English
Published: Nature Portfolio 2017-05-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-017-02455-z

Internet

https://doi.org/10.1038/s41598-017-02455-z

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