Whole‐exome sequencing identifies a novel mutation of GPD1L (R189X) associated with familial conduction disease and sudden death

Cardiac conduction disease (CCD) is a serious disorder and the leading cause of mortality worldwide. It is characterized by arrhythmia, syncope or even sudden cardiac death caused by the dysfunction of cardiac voltage‐gated channel. Previous study has demonstrated that mutations in genes encoding vo...

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Detalles Bibliográficos
Autores principales: Huang, Hao, Chen, Ya‐Qin, Fan, Liang‐Liang, Guo, Shuai, Li, Jing‐Jing, Jin, Jie‐Yuan, Xiang, Rong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Short Communications
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5783853/
https://www.ncbi.nlm.nih.gov/pubmed/29077258
http://dx.doi.org/10.1111/jcmm.13409

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5783853/
https://www.ncbi.nlm.nih.gov/pubmed/29077258
http://dx.doi.org/10.1111/jcmm.13409

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