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On Genetic and Phenotypic Variability of Hypertrophic Cardiomyopathy: Nature Versus Nurture
The seminal discovery of the R403Q mutation in the beta-myosin heavy chain (MyHC) gene as a cause of hypertrophic cardiomyopathy (HCM) by Dr. Thierfelder’s group a decade ago (1) ushered in a new era in the molecular genetics of HCM. To date, over 120 mutations in 10 genes, all encoding sarcomeric p...
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| Autor principal: | |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2001
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2900847/ https://ncbi.nlm.nih.gov/pubmed/11499720 |
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