S151A δ-sarcoglycan mutation causes a mild phenotype of cardiomyopathy in mice

So far, the role of mutations in the δ-sarcogylcan (Sgcd) gene in causing autosomal dominant dilated cardiomyopathy (DCM) remains inconclusive. A p.S151A missense mutation in exon 6 of the Sgcd gene was reported to cause severe isolated autosomal dominant DCM without affecting skeletal muscle. This...

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Detalhes bibliográficos
Main Authors: Rutschow, Désirée, Bauer, Ralf, Göhringer, Caroline, Bekeredjian, Raffi, Schinkel, Stefanie, Straub, Volker, Koenen, Michael, Weichenhan, Dieter, Katus, Hugo A, Müller, Oliver J
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group 2014
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3865419/
https://ncbi.nlm.nih.gov/pubmed/23695275
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2013.97
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