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Allele-specific Silencing of Mutant Myh6 Allele in Mice Suppresses Hypertrophic Cardiomyopathy

Dominant mutations in sarcomere proteins such as the myosin heavy chains (MHC) are the leading genetic causes of human hypertrophic cardiomyopathy (HCM) and dilated cardiomyopathy (DCM). Here we demonstrate that expression of the HCM cardiac MHC gene (Myh6) R403Q mutation in mice can be selectively...

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Detaylı Bibliyografya
Asıl Yazarlar: Jiang, Jianming, Wakimoto, Hiroko, Seidman, J. G., Seidman, Christine E.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2013
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC4100553/
https://ncbi.nlm.nih.gov/pubmed/24092743
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1126/science.1236921
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