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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...

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Shranjeno v:
Bibliografske podrobnosti
izdano v:Int J Mol Med
Main Authors: Zhao, Yue, Feng, Yue, Ding, Xiaoxue, Dong, Shuwei, Zhang, Hong, Ding, Jiahuan, Xia, Xueshan
Format: Artigo
Jezik:Inglês
Izdano: D.A. Spandidos 2017
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC5466385/
https://ncbi.nlm.nih.gov/pubmed/28498465
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/ijmm.2017.2986
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