Identification of a novel hypertrophic cardiomyopathy-associated mutation using targeted next-generation sequencing

Hypertrophic cardiomyopathy (HCM), one of the most common forms of myocardial diseases, is the major cause of sudden cardiac death in young adults and competitive athletes. Analyses of gene mutations associated with HCM are valuable for its molecular diagnosis, genetic counseling, and management of...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhao, Yue, Feng, Yue, Ding, Xiaoxue, Dong, Shuwei, Zhang, Hong, Ding, Jiahuan, Xia, Xueshan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2017
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5466385/
https://www.ncbi.nlm.nih.gov/pubmed/28498465
http://dx.doi.org/10.3892/ijmm.2017.2986

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5466385/
https://www.ncbi.nlm.nih.gov/pubmed/28498465
http://dx.doi.org/10.3892/ijmm.2017.2986

Ejemplares similares