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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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| Veröffentlicht in: | Int J Mol Med |
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| Hauptverfasser: | , , , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
D.A. Spandidos
2017
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| Schlagworte: | |
| Online Zugang: | 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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