Lack of MEF2A mutations in coronary artery disease

Mutations in MEF2A have been implicated in an autosomal dominant form of coronary artery disease (adCAD1). In this study we sought to determine whether severe mutations in MEF2A might also explain sporadic cases of coronary artery disease (CAD). To do this, we resequenced the coding sequence and spl...

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Detalhes bibliográficos
Main Authors: Weng, Li, Kavaslar, Nihan, Ustaszewska, Anna, Doelle, Heather, Schackwitz, Wendy, Hébert, Sybil, Cohen, Jonathan C., McPherson, Ruth, Pennacchio, Len A.
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Clinical Investigation 2005
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1070426/
https://ncbi.nlm.nih.gov/pubmed/15841183
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI200524186
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