MTHFR 677C→T mutation, folate intake, neural-tube defect, and risk of cardiovascular disease

This publication has 9 references indexed in Scilit:

• Disorders of homocysteine metabolism
  Journal of Inherited Metabolic Disease, 1997
• Thermolabile variant of 5, 10-methylenetetrahydrofolate reductaseassociated with low red-cell folates: implications for folate intake recommendations
  The Lancet, 1997
• Is the common 677C-->T mutation in the methylenetetrahydrofolate reductase gene a risk factor for neural tube defects? A meta-analysis
  QJM: An International Journal of Medicine, 1997
• Methylenetetrahydrofolate Reductase Gene and Coronary Artery Disease
  Circulation, 1997
• Methylenetetrahydrofolate Reductase Polymorphism, Plasma Folate, Homocysteine, and Risk of Myocardial Infarction in US Physicians
  Circulation, 1996
• Distribution in Healthy and Coronary Populations of the Methylenetetrahydrofolate Reductase (MTHFR) C ₆₇₇ T Mutation
  Arteriosclerosis, Thrombosis, and Vascular Biology, 1996
• A Quantitative Assessment of Plasma Homocysteine as a Risk Factor for Vascular Disease
  JAMA, 1995
• A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase
  Nature Genetics, 1995
• POSSIBLE PREVENTION OF NEURAL-TUBE DEFECTS BY PERICONCEPTIONAL VITAMIN SUPPLEMENTATION
  The Lancet, 1980