5-10 Methylenetetrahydrofolate reductase (MTFHR) 677C→T and 1298A→C mutations are associated with DNA hypomethylation
Castro R, Rivera I, Ravasco P, et al. 2004. 5-10 methylenetetrahydrofolate reductase (MTFHR) 677C→T and 1298A→C mutations are associated with DNA hypomethylation. J Med Genet 41: 454-458.
A common mutation in the 5,10-methylenetetrahydrofolate reductase gene affects genomic methylation through an interaction with folate status
Friso S, Choi S-W, Girelli D, et al. 2002. A common mutation in the 5,10-methylenetetrahydrofolate reductase gene affects genomic methylation through an interaction with folate status. Proc Natl Acacl Sci U S A 99: 5606-5611.
A candidate genetic risk factor for vascular disease: A common mutation in methylenetetrahydrofolate reductase
Frosst P, Blom HJ, Milos R, et al. 1995. A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase. Nat Genet 10: 111-113.
Incidence and significance of chromosome mosaicism involving an autosomal structural abnormality diagnosed prenatally through amniocentesis: A collaborative study
Hsu LYF, Yu M-T, Richkind KE, et al. 1996. Incidence and significance of chromosome mosaicism involving an autosomal structural abnormality diagnosed prenatally through amniocentesis: a collaborative study. Prenat Diagn 16: 1-28.
A second genetic polymorphism in methylenetetrahydrofolate reductase (MTHFR) associated with decreased enzyme activity
Weisberg I, Tran P, Christensen B, Sibani S, Rozen R. 1998. A second genetic polymorphism in methylenetetrahydrofolate reductase (MTHFR) associated with decreased enzyme activity. Mol Genet Metab 64: 169-172.
A common mutation in the methylenetetrahydrofolate reductase gene is a determinant of hyperhomocystinemia in epileptic patients receiving anticonvulsants
Yoo JH, Hong SB. 1999. A common mutation in the methylenetetrahydrofolate reductase gene is a determinant of hyperhomocystinemia in epileptic patients receiving anticonvulsants. Metabolism 48: 1047-1051.