Novel trigenic CACNA1C/DES/MYPN mutations in a family of hypertrophic cardiomyopathy with early repolarization and short QT syndrome

BACKGROUND: Hypertrophic cardiomyopathy (HCM) patients with early repolarization (ER) pattern are at higher risk of ventricular arrhythmia, yet the genetic background of this situation has not been well investigated. Here we report novel trigenic mutations detected in a Chinese family of obstructive...

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Detalles Bibliográficos
Autores principales: Chen, Yanhong, Barajas-Martinez, Hector, Zhu, Dongxiao, Wang, Xihui, Chen, Chonghao, Zhuang, Ruijuan, Shi, Jingjing, Wu, Xueming, Tao, Yijia, Jin, Weidong, Wang, Xiaoyan, Hu, Dan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5399316/
https://www.ncbi.nlm.nih.gov/pubmed/28427417
http://dx.doi.org/10.1186/s12967-017-1180-1

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