Lamin A/C Haploinsufficiency Causes Dilated Cardiomyopathy and Apoptosis-Triggered Cardiac Conduction System Disease

Mutations in the lamin A/C (LMNA) gene, which encodes nuclear membrane proteins, cause a variety of human conditions including dilated cardiomyopathy (DCM) with associated cardiac conduction system disease. To investigate mechanisms responsible for electrophysiologic and myocardial phenotypes caused...

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Detalhes bibliográficos
Main Authors: Wolf, Cordula M, Wang, Libin, Alcalai, Ronny, Pizard, Anne, Burgon, Patrick G, Ahmad, Ferhaan, Sherwood, Megan, Branco, Dorothy M, Wakimoto, Hiroko, Fishman, Glenn I, See, Vincent, Stewart, Colin L, Conner, David A, Berul, Charles I, Seidman, Christine E, Seidman, JG
Formato: Artigo
Idioma:Inglês
Publicado em: 2007
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3011813/
https://ncbi.nlm.nih.gov/pubmed/18182166
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.yjmcc.2007.11.008
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