A 19-Base Pair Deletion Polymorphism in Dihydrofolate Reductase Is Associated with Increased Unmetabolized Folic Acid in Plasma and Decreased Red Blood Cell Folate-Reference-Cited by-同舟云学术

A 19-Base Pair Deletion Polymorphism in Dihydrofolate Reductase Is Associated with Increased Unmetabolized Folic Acid in Plasma and Decreased Red Blood Cell Folate

Published:2008-12-01 Issue:12 Volume:138 Page:2323-2327
ISSN:0022-3166
Container-title:The Journal of Nutrition
language:en
Short-container-title:

Author:

Kalmbach Renee D.¹,Choumenkovitch Silvina F.¹,Troen Aron P.¹,Jacques Paul F.¹,D'Agostino Ralph²,Selhub Jacob¹

Affiliation:

1. Vitamin Metabolism and Aging Laboratory, Jean Mayer USDA Human Nutrition Research Center on Aging at Tufts University, Boston, MA 02111

2. Framingham Heart Study, Boston University School of Medicine, Framingham, MA 01701

Publisher

Oxford University Press (OUP)

Subject

Nutrition and Dietetics,Medicine (miscellaneous)

Link

http://academic.oup.com/jn/article-pdf/138/12/2323/24056175/2323.pdf

Reference39 articles.

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3. New 19 bp deletion polymorphism in intron-1 of dihydrofolate reductase (DHFR): a risk factor for spina bifida acting in mothers during pregnancy?;Johnson;Am J Med Genet A.,2004

4. The 19-bp deletion polymorphism in intron-1 of dihydrofolate reductase (DHFR) may decrease rather than increase risk for spina bifida in the Irish population;Parle-McDermott;Am J Med Genet A.,2007

5. Variation and expression of dihydrofolate reductase (DHFR) in relation to spina bifida;van der Linden;Mol Genet Metab.,2007

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