Lack of association between methylenetetrahydrofolate reductase (MTHFR) C677T and ischaemic heart disease (IHD): family-based association study in a Spanish population
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1034/j.1399-0004.2002.620309.x/fullpdf
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2. A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase;Frosst;Nat Genet,1995
3. Homocysteine and the MTHFR 677C → T allele in premature coronary artery disease. Case control and family studies;Pintó;Eur J Clin Invest,2001
4. Transmission test for linkage disequilibrium. the insulin gene region and insulin-dependent diabetes mellitus (IDDM);Spielman;Am J Hum Genet,1993
5. Genetic polymorphism of 5,10-methylenetetrahydrofolate reductase (MTHFR) as a risk factor for coronary artery disease;Morita;Circulation,1997
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1. Association between polymorphism of MTHFR c.677C>T and risk of cardiovascular disease in Turkish population: a meta-analysis for 2.780 cases and 3.022 controls;Molecular Biology Reports;2013-11-22
2. Physiologic changes in homocysteine metabolism in pregnancy: A longitudinal study in Spain;Nutrition;2011-09
3. E65 K polymorphism in KCNMB1 gene is not associated with ischaemic heart disease in Spanish patients;Journal of Human Genetics;2005-09-10
4. Homocysteine, Folic Acid, and Cardiovascular Disease Risk;Preventive Nutrition;2005
5. Frecuencia de la mutación 677C-T del gen de la metilentetrahidrofolato reductasa en una muestra de 652 recién nacidos de toda España;Medicina Clínica;2004-01
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