Does the polymorphism 677C-T of the 5,10-methylenetetrahydrofolate reductase gene contribute to homocysteine-related vascular disease?
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1023/A:1005414617390/fullpdf
Reference33 articles.
1. The mutation Ala-677-Val in the methylenetetrahydrofolate reductase gene: a risk factor for arterial disease and venous thrombosis;Arruda;T hromb Haemost,1997
2. Heterozygosity for homocystinuria in premature peripheral and cerebral occlusive arterial disease;Boers;N Engl J Med,1985
3. The thermolabile methylenetetrahydrofolate reductase (MTHFR) mutation-a common finding in the UK population;Bonham;J Inher Metab Dis,1996
4. A common mutation in methylenetetrahydrofolate reductase gene is not a major risk of coronary artery disease or myocardial infarction;Brugada;Atherosclerosis,1997
5. Rapid determination of total homocysteine in plasma;Chadefaux;Clin Chem,1989
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