Investigations of a common genetic variant in betaine–homocysteine methyltransferase (BHMT) in coronary artery disease-Reference-Cited by-同舟云学术

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Investigations of a common genetic variant in betaine–homocysteine methyltransferase (BHMT) in coronary artery disease

Published:2003-04 Issue:2 Volume:167 Page:205-214
ISSN:0021-9150
Container-title:Atherosclerosis
language:en
Short-container-title:Atherosclerosis

Author:

Weisberg Ilan S.,Park Eric,Ballman Karla V.,Berger Peter,Nunn Martha,Suh Daniel S.,Breksa Andrew P.,Garrow Timothy A.,Rozen Rima

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine

Reference31 articles.

1. A quantitative assessment of plasma homocysteine as a risk factor for vascular disease;Boushey;J. Am. Med. Assoc.,1995

2. Homocysteine and cardiovascular disease;Refsum;Ann. Rev. Med.,1998

3. A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase;Frosst;Nat. Genet.,1995

4. The 1298A→C polymorphism in methylenetetrahydrofolate reductase (MTHFR): in vitro expression and association with homocysteine;Weisberg;Atherosclerosis,2001

5. Relation between folate status, a common mutation in methylenetetrahydrofolate reductase, and plasma homocysteine concentrations;Jacques;Circulation,1996

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