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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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Autors principals: | , , , , , , , , |
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Format: | Artigo |
Idioma: | Inglês |
Publicat: |
American Society for Clinical Investigation
2005
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Matèries: | |
Accés en línia: | 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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