Diastolic dysfunction in familial hypertrophic cardiomyopathy transgenic model mice

AIMS: Several mutations in the ventricular myosin regulatory light chain (RLC) were identified to cause familial hypertrophic cardiomyopathy (FHC). Based on our previous cellular findings showing delayed calcium transients in electrically stimulated intact papillary muscle fibres from transgenic Tg-...

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Detalhes bibliográficos
Main Authors: Abraham, Theodore P., Jones, Michelle, Kazmierczak, Katarzyna, Liang, Hsin-Yueh, Pinheiro, Aurelio C., Wagg, Cory S., Lopaschuk, Gary D., Szczesna-Cordary, Danuta
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2009
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Original Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2721639/
https://ncbi.nlm.nih.gov/pubmed/19150977
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/cvr/cvp016
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