The embryological basis of subclinical hypertrophic cardiomyopathy

Hypertrophic cardiomyopathy (HCM) is caused by mutations in sarcomeric proteins, the commonest being MYBPC3 encoding myosin-binding protein C. It is characterised by left ventricular hypertrophy but there is an important pre-hypertrophic phenotype with features including crypts, abnormal mitral leaf...

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發表在:Sci Rep
Main Authors: Captur, Gabriella, Ho, Carolyn Y., Schlossarek, Saskia, Kerwin, Janet, Mirabel, Mariana, Wilson, Robert, Rosmini, Stefania, Obianyo, Chinwe, Reant, Patricia, Bassett, Paul, Cook, Andrew C., Lindsay, Susan, McKenna, William J., Mills, Kevin, Elliott, Perry M., Mohun, Timothy J., Carrier, Lucie, Moon, James C.
格式: Artigo
語言:Inglês
出版: Nature Publishing Group 2016
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Article
在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC4914973/
https://ncbi.nlm.nih.gov/pubmed/27323879
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/srep27714
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