A common mutation in the methylenetetrahydrofolate reductase gene is associated with an accumulation of formylated tetrahydrofolates in red blood cells-Reference-Cited by-同舟云学术

A common mutation in the methylenetetrahydrofolate reductase gene is associated with an accumulation of formylated tetrahydrofolates in red blood cells

Published:1998-10-27 Issue:22 Volume:95 Page:13217-13220
ISSN:0027-8424
Container-title:Proceedings of the National Academy of Sciences
language:en
Short-container-title:Proceedings of the National Academy of Sciences

Author:

Bagley P. J.,Selhub J.

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

Reference26 articles.

1. The pathogenesis of homocysteinemia: interruption of the coordinate regulation by S-adenosylmethionine of the remethylation and transsulfuration of homocysteine

2. Human methylenetetrahydrofolate reductase: isolation of cDNA, mapping and mutation identification

3. Folate Distribution in Cultured Human Cells

4. Genetic Predisposition to Hyperhomocysteinemia: Deficiency of Methylenetetrahydrofolate Reductase (MTHFR)

5. A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase

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