
Functional genetic variants in the SIRT5 gene promoter in acute myocardial infarction
Keywords: AMI; acute myocardial infarction; CAD; coronary artery disease; CEBPB; CCAAT/enhancer binding protein β; DSVs; DNA sequence variants; EMSA; electrophoretic mobility shift assay; FOXC1; forkhead box C1; H9c2; rat cardiomyocyte line; HEK-293; human embryon