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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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| Publicado no: | Int J Mol Med |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
D.A. Spandidos
2017
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| Assuntos: | |
| Acesso em linha: | 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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