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29. Association of methylenetetrahydrofolate reductase gene polymorphism with carotid arterial wall thickening and myocardial infarction risk in NIDDM. Arai K; Yamasaki Y; Kajimoto Y; Watada H; Umayahara Y; Kodama M; Sakamoto K; Hori M Diabetes; 1997 Dec; 46(12):2102-4. PubMed ID: 9392503 [No Abstract] [Full Text] [Related]
30. Mutation C677T of methylenetetrahydrofolate reductase gene is not associated with coronary artery disease, but possibly with albuminuria, in type 2 diabetic patients. Wirta V; Huang XH; Wirta O; Rantalaiho V; Pasternack A; Jokela H; Koivula T; Lehtimäki T Clin Chem Lab Med; 1998 Aug; 36(8):625-8. PubMed ID: 9806473 [TBL] [Abstract][Full Text] [Related]
31. The 677 C-->T mutation in the methylenetetrahydrofolate reductase (MTHFR) gene in five Chinese ethnic groups. Yu J; Chen B; Zhang G; Fu S; Li P Hum Hered; 2000; 50(4):268-70. PubMed ID: 10782023 [No Abstract] [Full Text] [Related]
33. Plasma homocysteine, methylenetetrahydrofolate reductase genotypes, and age at onset of symptoms of myocardial ischemia. Mager A; Battler A; Birnbaum Y; Magal N; Shohat M Am J Cardiol; 2002 Apr; 89(8):919-23. PubMed ID: 11950428 [TBL] [Abstract][Full Text] [Related]
34. Common mutation in the methylenetetrahydrofolate reductase gene offers no support for mild hyperhomocysteinemia being a causal risk factor for cardiovascular disease. Brattström L Circulation; 1997 Nov; 96(10):3805-7. PubMed ID: 9396508 [No Abstract] [Full Text] [Related]
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38. Homocysteine, MTHFR 677C-->T polymorphism, and risk of ischemic stroke: results of a meta-analysis. Fallon UB; Ben-Shlomo Y Neurology; 2003 Feb; 60(3):526-7; author reply 526-7. PubMed ID: 12578952 [No Abstract] [Full Text] [Related]
39. Genetic variation of the methylenetetrahydrofolate reductase and cystathionine beta-synthase genes in Korean patients with coronary artery disease and a new polymorphism in intron 7. Hong SH; Song J; Kim JQ Mol Cell Probes; 2001 Apr; 15(2):119-23. PubMed ID: 11292330 [TBL] [Abstract][Full Text] [Related]