Unequal allelic expression of wild-type and mutated β-myosin in familial hypertrophic cardiomyopathy

Familial hypertrophic cardiomyopathy (FHC) is an autosomal dominant disease, which in about 30% of the patients is caused by missense mutations in one allele of the β-myosin heavy chain (β-MHC) gene (MYH7). To address potential molecular mechanisms underlying the family-specific prognosis, we determ...

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Detalhes bibliográficos
Main Authors: Tripathi, Snigdha, Schultz, Imke, Becker, Edgar, Montag, Judith, Borchert, Bianca, Francino, Antonio, Navarro-Lopez, Francisco, Perrot, Andreas, Özcelik, Cemil, Osterziel, Karl-Josef, McKenna, William J., Brenner, Bernhard, Kraft, Theresia
Formato: Artigo
Idioma:Inglês
Publicado em: Springer-Verlag 2011
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Original Contribution
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3228959/
https://ncbi.nlm.nih.gov/pubmed/21769673
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00395-011-0205-9
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