A Common Mutation A1298C in Human Methylenetetrahydrofolate Reductase Gene: Association with Plasma Total Homocysteine and Folate Concentrations-Reference-Cited by-同舟云学术

A Common Mutation A1298C in Human Methylenetetrahydrofolate Reductase Gene: Association with Plasma Total Homocysteine and Folate Concentrations

Published:1999-09-01 Issue:9 Volume:129 Page:1656-1661
ISSN:0022-3166
Container-title:The Journal of Nutrition
language:en
Short-container-title:

Author:

Friedman Gideon¹,Goldschmidt Netta¹,Friedlander Yechiel²,Ben-Yehuda Arie¹,Selhub Jacob³,Babaey Sharona¹,Mendel Malka²,Kidron Miriam⁴,Bar-On Hanoch⁴

Affiliation:

1. Geriatric Unit, Lipid Research Laboratory

2. Department of Social Medicine, School of Public Health and Community Medicine

3. Jean Mayer U.S. Department of Agriculture Human Nutrition Research Center, Tufts, New England Medical Center, Boston, MA

4. Diabetes Unit, Hebrew University Hadassah Medical Center, Jerusalem, Israel

Publisher

Oxford University Press (OUP)

Subject

Nutrition and Dietetics,Medicine (miscellaneous)

Link

http://academic.oup.com/jn/article-pdf/129/9/1656/24026870/4w099901656.pdf

Reference40 articles.

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2. Determination of free and total homocysteine in human plasma by high-performance liquid chromatography with fluorescence detection;Araki;J. Chromatogr.,1987

3. The mutation ala677val in the methylenetetrahydrofolate reductase gene: A risk factor for arterial disease and venous thrombosis;Arruda;Thomb. Haemost.,1997

4. Hyperhomocysteinaemia and associated disease;Bakker;Phan. World. Sci.,1997

5. Serum glucose and insulin characteristics and prevalence of diabetes mellitus and impaired glucose tolerance in the adult Jewish population of Jerusalem;Bar-On;Nutr. Metab. Cardiovasc. Dis.,1992

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