A hemochromatosis-causing mutation C282Y is a risk factor for proliferative diabetic retinopathy in Caucasians with type 2 diabetes - Peterlin, Borut; Globočnik Petrovič, Mojca; Makuc, Jana; Hawlina, Marko; Petrovič, Daniel (Journal of human genetics, 2003)
Keywords: Aged; Biomedicine; Diabetes; Diabetes mellitus (non-insulin dependent); Diabetes Mellitus, Type 2 - complications; Diabetes Mellitus, Type 2 - genetics; Diabetic retinopathy; Diabetic Retinopathy - complications; Female; Gene Expression; Gene Function; Gene Therapy; Genetic Predisposition to Disease; Genotype; Genotypes; Hemochromatosis; Hemochromatosis - genetics; Heterozygote; Heterozygotes; Human Genetics; Humans; Male; Middle Aged; Molecular Medicine; Mutation; Odds Ratio; Original Article; Pathogenesis; Regression Analysis; Retinopathy; Risk Factors; White people; Hereditary hemochromatosis; Type 2 diabetes; C282Y mutation; Proliferative diabetic retinopathy