Items for "coronary artery diseases"
Background: Recently, a mutation in the human myocyte enhancer factor-2A (MEF2A) gene was reported to be responsible for an autosomal dominant form of coronary artery disease (CAD)...
Keywords: CAG repeat, coronary artery diseases, myocyte enhancer factor-2A (MEF2A), Polymorphism
08/2007 | Clinical Chemical Laboratory Medicine, Walter de Gruyter