Molecular basis for clinical heterogeneity in inherited cardiomyopathies due to myopalladin mutations

Abnormalities in Z-disc proteins cause hypertrophic (HCM), dilated (DCM) and/or restrictive cardiomyopathy (RCM), but disease-causing mechanisms are not fully understood. Myopalladin (MYPN) is a Z-disc protein expressed in striated muscle and functions as a structural, signaling and gene expression...

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Main Authors: Purevjav, Enkhsaikhan, Arimura, Takuro, Augustin, Sibylle, Huby, Anne-Cecile, Takagi, Ken, Nunoda, Shinichi, Kearney, Debra L., Taylor, Michael D., Terasaki, Fumio, Bos, Johan M., Ommen, Steve R., Shibata, Hiroki, Takahashi, Megumi, Itoh-Satoh, Manatsu, McKenna, William J., Murphy, Ross T., Labeit, Siegfried, Yamanaka, Yoichi, Machida, Noboru, Park, Jeong-Euy, Alexander, Peta M.A., Weintraub, Robert G., Kitaura, Yasushi, Ackerman, Michael J., Kimura, Akinori, Towbin, Jeffrey A.
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2012
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Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3315208/
https://ncbi.nlm.nih.gov/pubmed/22286171
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/dds022
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