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Hypertrophic cardiomyopathy: Translating cellular cross talk into therapeutics

Hypertrophic cardiomyopathy (HCM) is a common inherited heart disease with serious adverse outcomes, including heart failure, arrhythmias, and sudden cardiac death. The discovery that mutations in sarcomere protein genes cause HCM has enabled the development of mouse models that recapitulate clinica...

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Autori principali: Teekakirikul, Polakit, Padera, Robert F., Seidman, J.G., Seidman, Christine E.
Natura: Artigo
Lingua:Inglês
Pubblicazione: The Rockefeller University Press 2012
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC3483129/
https://ncbi.nlm.nih.gov/pubmed/23109667
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1083/jcb.201207033
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