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Volumn 13, Issue 5, 2002, Pages 423-431

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

Author keywords

Acquired risk factors; Factor V Leiden; G20210A prothrombin gene variant; Homocysteine; MTHFR gene polymorphisms; Venous thromboembolic disease

Indexed keywords

5,10 METHYLENETETRAHYDROFOLATE REDUCTASE (FADH2); ALANINE; CYSTEINE; HOMOCYSTEINE; THREONINE;

EID: 0036630169     PISSN: 09575235     EISSN: None     Source Type: Journal    
DOI: 10.1097/00001721-200207000-00007     Document Type: Article
Times cited : (54)

References (52)
  • 19
    • 0035057410 scopus 로고    scopus 로고
    • C677T and A1298C polymorphisms of the methylenetetrahydrofolate reductase gene: Incidence and effect of combined genotypes on plasma fasting and postmethionine load homocysteine in vascular disease
    • (2001) Clin Chem , vol.47 , pp. 661-666
    • Hanson, N.Q.1    Aras, O.2    Yang, F.3    Tsai, M.Y.4
  • 27
    • 0031955592 scopus 로고    scopus 로고
    • Factor V Leiden (G1691A), the prothrombin 3′-untranslated region variant (G20210A) and thermolabile methylenetetrahydrofolate reductase (C677T): A single genetic test genotypes all three loci determination of frequencies in the S. Wales population of the UK
    • (1998) Thromb Haemost , vol.79 , pp. 949-954
    • Bowen, D.J.1    Bowley, S.2    John, M.3    Collins, P.W.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.