The Mitochondrial T16189C Polymorphism Is Associated with Coronary Artery Disease in Middle European Populations - Mueller, Edith E.; Eder, Waltraud; Ebner, Sabine; Schwaiger, Eva; Santic, Danijela; Kreindl, Tanja; Stanger, Olaf; Paulweber, Bernhard; Iglseder, Bernhard; Oberkofler, Hannes; Maier, Richard; Mayr, Johannes A.; et al. (PloS one, 2011)
Keywords: Age related diseases; Analysis; Apoptosis; Biology; Birth weight; Body mass; Body mass index; Body size; Cardiovascular disease; Case-Control Studies; Chi-square test; Coronary artery; Coronary artery disease; Coronary Artery Disease - genetics; Coronary heart disease; Coronary vessels; Deoxyribonucleic acid; Diabetes; Diabetes mellitus; Diabetes Mellitus, Type 2 - genetics; DNA; DNA damage; DNA sequencing; DNA, Mitochondrial - genetics; Europe - epidemiology; European Continental Ancestry Group - genetics; Gene expression; Gene sequencing; Genetic aspects; Genetic polymorphisms; Genetic Predisposition to Disease; Genomes; Genomics; Heart diseases; Heart failure; Humans; Insulin resistance; Internal medicine; Laboratories; Medical research; Medicine; Metabolic disorders; Mitochondria; Mitochondrial DNA; Mutation; Patients; Pediatrics; Polymorphism; Polymorphism, Single Nucleotide; Prostate cancer; Type 2 diabetes; Europe