Skeletal muscle expression and abnormal function of beta-myosin in hypertrophic cardiomyopathy.
Hypertrophic cardiomyopathy is an important inherited disease. The phenotype has been linked, in some kindreds, to the beta-myosin heavy chain (beta-MHC) gene. Missense and silent mutations in the beta-MHC gene were used as markers to demonstrate the expression of mutant and normal cardiac beta-MHC...
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| 發表在: | J Clin Invest |
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| Principais autores: | , , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
American Society for Clinical Investigation
1993
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC443355/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/8514894/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI116530 |
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