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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Autors principals: 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
Format: Artigo
Idioma:Inglês
Publicat: 2007
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Article
Accés en línia: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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