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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...

詳細記述

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書誌詳細
主要な著者: Teekakirikul, Polakit, Padera, Robert F., Seidman, J.G., Seidman, Christine E.
フォーマット: Artigo
言語:Inglês
出版事項: The Rockefeller University Press 2012
主題:
オンライン・アクセス: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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