Sporadic hypertrophic cardiomyopathy due to de novo myosin mutations.
Hypertrophic cardiomyopathy occurs as an autosomal dominant familial disorder or as a sporadic disease without familial involvement. While missense mutations in the beta cardiac myosin heavy chain (MHC) gene account for approximately half of all cases of familial hypertrophic cardiomyopathy, the mol...
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| Veröffentlicht in: | J Clin Invest |
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| Hauptverfasser: | , , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
American Society for Clinical Investigation
1992
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| Schlagworte: | |
| Online-Zugang: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC443222/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/1430197/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI116038 |
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