Myosin regulatory light chain mutation found in hypertrophic cardiomyopathy patients increases isometric force production in transgenic mice

FHC (familial hypertrophic cardiomyopathy) is a heritable form of cardiac hypertrophy caused by mutations in genes encoding sarcomeric proteins. The present study focuses on the A13T mutation in the human ventricular myosin RLC (regulatory light chain) that is associated with a rare FHC variant defi...

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Detalhes bibliográficos
Publicado no:Biochem J
Main Authors: Kazmierczak, Katarzyna, Muthu, Priya, Huang, Wenrui, Jones, Michelle, Wang, Yingcai, Szczesna-Cordary, Danuta
Formato: Artigo
Idioma:Inglês
Publicado em: 2012
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6589164/
https://ncbi.nlm.nih.gov/pubmed/22091967
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1042/BJ20111145
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