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Genetic Dissection of Hypertrophic Cardiomyopathy with Myocardial RNA-Seq
Hypertrophic cardiomyopathy (HCM) is an inherited disorder of the myocardium, and pathogenic mutations in the sarcomere genes myosin heavy chain 7 (MYH7) and myosin-binding protein C (MYBPC3) explain 60%–70% of observed clinical cases. The heterogeneity of phenotypes observed in HCM patients, howeve...
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| Publicado en: | Int J Mol Sci |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
MDPI
2020
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7246737/ https://ncbi.nlm.nih.gov/pubmed/32344918 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms21093040 |
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