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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...
Tallennettuna:
| Päätekijät: | , , , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
The Rockefeller University Press
2012
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| Aiheet: | |
| Linkit: | 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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