Nesprin-1 mutations in human and murine cardiomyopathy

Mutations in LMNA, the gene encoding the nuclear membrane proteins, lamins A and C, produce cardiac and muscle disease. In the heart, these autosomal dominant LMNA mutations lead to cardiomyopathy frequently associated with cardiac conduction system disease. Herein, we describe a patient with the R3...

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Main Authors: Puckelwartz, Megan J., Kessler, Eric J., Kim, Gene, DeWitt, Megan M., Zhang, Yuan, Earley, Judy U., Depreux, Frederic F.S., Holaska, James, Mewborn, Stephanie K., Pytel, Peter, McNally, Elizabeth M.
Formato: Artigo
Idioma:Inglês
Publicado: 2009
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Article
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC2837775/
https://ncbi.nlm.nih.gov/pubmed/19944109
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.yjmcc.2009.11.006
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