The C677T mutation in the methylenetetrahydrofolate reductase gene and its association with deep vein thrombophilia in Shandong Hans

Chinese Journal of Medical Genetics

Volumn 19, Issue 4, 2002, Pages 295-297

  Guo, Chenhong ^a   Guo, Qiongxing ^a   Gong, Yaoqin ^a   Chen, Bingxi ^a   Liu, Qiji ^a   Li, Jiangxia ^a   Gao, Guimin ^a   Zhou, Haibin ^a  

^a SHANDONG UNIVERSITY SCHOOL OF MEDICINE   (China)

Author keywords

Deep vein thrombophilia; Gene mutation; Methylenetetrahydrofolate reductase gene

Indexed keywords

GENES; PATIENT MONITORING;

POLYMORPHISM;

GENETIC ENGINEERING;

5,10 METHYLENETETRAHYDROFOLATE REDUCTASE (FADH2);

ARTICLE; CHINA; CONTROLLED STUDY; DEEP VEIN THROMBOSIS; GENE FREQUENCY; GENE MUTATION; GENETIC ASSOCIATION; GENOTYPE; HETEROZYGOTE; HUMAN; MAJOR CLINICAL STUDY; PREVALENCE; RISK FACTOR;

CHINA; DNA; GENE FREQUENCY; GENOTYPE; HUMANS; METHYLENETETRAHYDROFOLATE REDUCTASE (NADPH2); ODDS RATIO; OXIDOREDUCTASES ACTING ON CH-NH GROUP DONORS; POINT MUTATION; POLYMORPHISM, RESTRICTION FRAGMENT LENGTH; THROMBOPHILIA; VENOUS THROMBOSIS;

EID: 0036684679     PISSN: 10039406     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (10)

1. The mutation Ala 677 Val in the methylenetetrahydrofolate reductase gene: A risk factor for arterial disease and venous thrombosis
2. A candidate genetic risk factor for vascular disease: A common mutation in methylenetetrahydrofolate reductase
3. Nutritional ecogenetics: Homocysteine-related arteriosclerotic vascular disease, neutral tube defect, and folic acid
4. Relationship between homocysteine and thrombotic disease
5. The prevalence of C677T methylenetrahydrofolate reductase gene and its association with venous thrombophilia in Taiwanese Chinese