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

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 inve...

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Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5445094/
https://www.ncbi.nlm.nih.gov/pubmed/28546535
http://dx.doi.org/10.1038/s41598-017-02455-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5445094/
https://www.ncbi.nlm.nih.gov/pubmed/28546535
http://dx.doi.org/10.1038/s41598-017-02455-z

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