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Article

V677 mutation of methylenetetrahydrofolate reductase and cardiovascular disease in Canadian Inuit

1 Apr 1997

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 9130949
DOI: 10.1016/s0140-6736(05)62414-2

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Related research

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V677 mutation of methylenetetrahydrofolate reductase and cardiovascular disease in Canadian InuitPMID 9130949Read ↗

Mutated 5,10-methylenetetrahydrofolate reductase, hyperhomocysteinemia and risk for cardiovascular disease. Nature, nurture or nonsense?Semantic proximity Read ↗

A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductaseSemantic proximity Read ↗

A1298C methylenetetrahydrofolate reductase mutation and coronary artery disease: relationships with C677T polymorphism and homocysteine/folate metabolism.Semantic proximity Read ↗

Prospective study of methylenetetrahydrofolate reductase (MTHFR) variant C677T and risk of all-cause and cardiovascular disease mortality among 6000 US adultsSemantic proximity Read ↗

Association of the C677T methylenetetrahydrofolate reductase mutation and elevated homocysteine levels with congenital cardiac malformationsSemantic proximity Read ↗

Methylene tetrahydrofolate reductase mutation and stroke in a monozygotic twin.Semantic proximity Read ↗

Methylenetetrahydrofolate reductase C677T polymorphism and diabetic retinopathy.Semantic proximity Read ↗

[Role of polymorphic variants of the 5,10-methylenetetrahydrofolate reductase (MTHFR) gene in the pathogenesis of cardiovascular diseases].Semantic proximity Read ↗

A common mutation in the methylenetetrahydrofolate reductase gene and risk of coronary heart disease: results among U.S. men.Semantic proximity Read ↗

Association of genetic variants in Methylenetetrahydrofolate Reductase and Paraoxonase-1 genes with homocysteine, folate and vitamin B12 in coronary artery diseaseSemantic proximity Read ↗

Methylene tetrahydrofolate reductase C677T polymorphism in Korean livedoid vasculopathy patients.Semantic proximity Read ↗

Methylenetetrahydrofolate reductase gene C677T and A1298C polymorphisms, plasma homocysteine, folate, and vitamin B12 levels and the extent of coronary artery diseaseSemantic proximity Read ↗

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