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Identifying Sarcomere Gene Mutations in HCM: A Personal History

This article provides an historical and personal perspective on the discovery of genetic causes for hypertrophic cardiomyopathy (HCM). Extraordinary insights of physicians who initially detailed remarkable and varied manifestations of the disorder, collaboration among multidisciplinary teams with sk...

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Detalhes bibliográficos
Main Authors: Seidman, Christine E., Seidman, J.G.
Formato: Artigo
Idioma:Inglês
Publicado em: 2011
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3072749/
https://ncbi.nlm.nih.gov/pubmed/21415408
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1161/CIRCRESAHA.110.223834
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