Lamin A/C mutation analysis in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy

BACKGROUND: Lamin A/C mutations are a well established cause of dilated cardiomyopathy (DCM), although their frequency has not been examined in a large cohort of patients.We sought to examine the frequency of mutations in LMNA, the gene encoding lamin A/C, in patients with idiopathic (IDC) or famili...

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Detalhes bibliográficos
Main Authors: Parks, Sharie B., Kushner, Jessica D., Nauman, Deirdre, Burgess, Donna, Ludwigsen, Susan, Peterson, Amanda, Li, Duanxiang, Jakobs, Petra, Litt, Michael, Porter, Charles B., Rahko, Peter S., Hershberger, Ray E.
Formato: Artigo
Idioma:Inglês
Publicado em: 2008
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2527054/
https://ncbi.nlm.nih.gov/pubmed/18585512
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ahj.2008.01.026
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