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Modifier genes for hypertrophic cardiomyopathy
During the past decade, more than 100 mutations in 11 causal gene coding for sarcomeric proteins, the γ subunit of AMP-activated protein kinase and triplet-repeat syndromes and in mitochondrial DNA, have been identified in patients with hypertrophic cardiomyopathy (HCM). Genotype–phenotype correlati...
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2002
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2775140/ https://ncbi.nlm.nih.gov/pubmed/12015473 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/01.HCO.0000013803.40803.6A |
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