Hypertrophic cardiomyopathy clinical phenotype is independent of gene mutation and mutation dosage

Over 1,500 gene mutations are known to cause hypertrophic cardiomyopathy (HCM). Previous studies suggest that cardiac β-myosin heavy chain (MYH7) gene mutations are commonly associated with a more severe phenotype, compared to cardiac myosin binding protein-C (MYBPC3) gene mutations with milder phen...

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Detalhes bibliográficos
Publicado no:PLoS One
Main Authors: Viswanathan, Shiv Kumar, Sanders, Heather K., McNamara, James W., Jagadeesan, Aravindakshan, Jahangir, Arshad, Tajik, A. Jamil, Sadayappan, Sakthivel
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2017
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5679632/
https://ncbi.nlm.nih.gov/pubmed/29121657
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0187948
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