Whole exome sequencing identifies a KCNJ12 mutation as a cause of familial dilated cardiomyopathy

Dilated cardiomyopathy (DCM) is characterized by left ventricular dilation, and is associated with systolic dysfunction and increased action potential duration. Approximately 50% of DCM cases are caused by inherited gene mutations with genetic and phenotypic heterogeneity. Next generation sequencing...

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Detalhes bibliográficos
Publicado no:Medicine (Baltimore)
Main Authors: Yuan, Hai-Xin, Yan, Kai, Hou, Dong-Yan, Zhang, Zhi-Yong, Wang, Hua, Wang, Xin, Zhang, Juan, Xu, Xiao-Rong, Liang, Yan-Hong, Zhao, Wen-Shu, Xu, Lin, Zhang, Lin
Formato: Artigo
Idioma:Inglês
Publicado em: Wolters Kluwer Health 2017
Assuntos:
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5571686/
https://ncbi.nlm.nih.gov/pubmed/28816949
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/MD.0000000000007727
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