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Volumn 13, Issue 5, 2002, Pages 423-431
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Mutations C677T and A1298C of the 5,10-methylenetetrahydrofolate reductase gene and fasting plasma homocysteine levels are not associated with the increased risk of venous thromboembolic disease
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Author keywords
Acquired risk factors; Factor V Leiden; G20210A prothrombin gene variant; Homocysteine; MTHFR gene polymorphisms; Venous thromboembolic disease
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Indexed keywords
5,10 METHYLENETETRAHYDROFOLATE REDUCTASE (FADH2);
ALANINE;
CYSTEINE;
HOMOCYSTEINE;
THREONINE;
AGED;
ARTICLE;
CONTROLLED STUDY;
DIET RESTRICTION;
FEMALE;
GENE FREQUENCY;
GENE MUTATION;
GENETIC POLYMORPHISM;
GENETIC STRAIN;
GENOTYPE;
HETEROZYGOTE;
HUMAN;
MAJOR CLINICAL STUDY;
MALE;
PRIORITY JOURNAL;
RISK FACTOR;
THROMBOEMBOLISM;
VEIN THROMBOSIS;
3' UNTRANSLATED REGIONS;
ACTIVATED PROTEIN C RESISTANCE;
ADOLESCENT;
ADULT;
AGED;
AGED, 80 AND OVER;
ALLELES;
AMINO ACID SUBSTITUTION;
CODON;
FACTOR V;
FASTING;
FEMALE;
GENE FREQUENCY;
GENETIC PREDISPOSITION TO DISEASE;
GENOTYPE;
HOMOCYSTEINE;
HUMANS;
HYPERHOMOCYSTEINEMIA;
MALE;
METHYLENETETRAHYDROFOLATE REDUCTASE (NADPH2);
MIDDLE AGED;
MUTATION, MISSENSE;
OXIDOREDUCTASES ACTING ON CH-NH GROUP DONORS;
POINT MUTATION;
POLAND;
PROTHROMBIN;
RISK FACTORS;
THROMBOPHILIA;
VENOUS THROMBOSIS;
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EID: 0036630169
PISSN: 09575235
EISSN: None
Source Type: Journal
DOI: 10.1097/00001721-200207000-00007 Document Type: Article |
Times cited : (54)
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References (52)
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