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Inherited cardiomyopathies caused by troponin mutations
Genetic investigations of cardiomyopathy in the recent two decades have revealed a large number of mutations in the genes encoding sarcomeric proteins as a cause of inherited hypertrophic cardiomyopathy (HCM), dilated cardiomyopathy (DCM), or restrictive cardiomyopathy (RCM). Most functional analyse...
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| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Science Press
2013
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3627712/ https://ncbi.nlm.nih.gov/pubmed/23610579 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3969/j.issn.1671-5411.2013.01.014 |
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