The methylenetetrahydrofolate reductase C677T gene mutation is associated with hyperhomocysteinemia, cardiovascular disease and plasma B-type natriuretic peptide levels in Korea-Reference-Cited by-同舟云学术

The methylenetetrahydrofolate reductase C677T gene mutation is associated with hyperhomocysteinemia, cardiovascular disease and plasma B-type natriuretic peptide levels in Korea

Published:2006-01-01 Issue:9 Volume:44 Page:
ISSN:1434-6621
Container-title:Clinical Chemistry and Laboratory Medicine (CCLM)
language:
Short-container-title:

Author:

Cho Sung Eun,Sook Hong Ki,Shin Gil Ja,Chung Wha Soon

Abstract

AbstractClin Chem Lab Med 2006;44:1070–5.

Publisher

Walter de Gruyter GmbH

Subject

Biochemistry, medical,Clinical Biochemistry,General Medicine

Link

https://www.degruyter.com/document/doi/10.1515/CCLM.2006.194/pdf

Reference35 articles.

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3. Heterozygous methylenetetrahydrofolate reductase mutation with mild hyperhomocysteinemia associated with deep vein thrombosis;Pathare;Clin Lab Haematol,2004

4. The interaction between MTHFR genotype and folate status is a determinant of coronary atherosclerosis risk;Girelli;J Nutr,2003

5. Gene - nutrition interactions in coronary artery disease : correlation between the MTHFR polymorphism and folate and homocysteine status in a Korean population;Huh;Thromb Res,2006

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