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Volumn 3, Issue 9, 2005, Pages 2126-2127

An Arab selective gradient in the distribution of factor V G1691A (Leiden), prothrombin G20210A, and methylenetetrahydrofolate reductase (MTHFR) C677T [13]

Author keywords

[No Author keywords available]

Indexed keywords

5,10 METHYLENETETRAHYDROFOLATE REDUCTASE (FADH2); BLOOD CLOTTING FACTOR 5; PROTHROMBIN;

EID: 30644474960     PISSN: 15387933     EISSN: 15387836     Source Type: Journal    
DOI: 10.1111/j.1538-7836.2005.01546.x     Document Type: Letter
Times cited : (22)

References (12)
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    • A common genetic variation in the 3′-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis
    • Poort SR, Rosendaal FR, Reitsma PH, Bertina RM. A common genetic variation in the 3′-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis. Blood 1996; 88: 3698-703.
    • (1996) Blood , vol.88 , pp. 3698-3703
    • Poort, S.R.1    Rosendaal, F.R.2    Reitsma, P.H.3    Bertina, R.M.4
  • 4
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    • Prevalence of two thrombophilia predisposing mutations: Factor V G1691A (R506Q; Leiden) and prothrombin G20210A, among healthy Lebanese
    • Tamim H, Finan RR, Almawi WY. Prevalence of two thrombophilia predisposing mutations: factor V G1691A (R506Q; Leiden) and prothrombin G20210A, among healthy Lebanese. Thromb Haemost 2002; 88: 691-2.
    • (2002) Thromb Haemost , vol.88 , pp. 691-692
    • Tamim, H.1    Finan, R.R.2    Almawi, W.Y.3
  • 6
    • 0036178211 scopus 로고    scopus 로고
    • The frequent 5,10-methylenetetrahydrofolate reductase C677T polymorphism is associated with a common haplotype in whites, Japanese, and Africans
    • Rosenberg N, Murata M, Ikeda Y, Opare-Sem O, Zivelin A, Geffen E, Seligsohn U. The frequent 5,10-methylenetetrahydrofolate reductase C677T polymorphism is associated with a common haplotype in whites, Japanese, and Africans. Am J Hum Genet 2002; 70: 758-62.
    • (2002) Am J Hum Genet , vol.70 , pp. 758-762
    • Rosenberg, N.1    Murata, M.2    Ikeda, Y.3    Opare-Sem, O.4    Zivelin, A.5    Geffen, E.6    Seligsohn, U.7
  • 7
    • 0031202097 scopus 로고    scopus 로고
    • High frequency of the C677T mutation in the methylenetetrahydrofolate reductase (MTHFR) gene in Northern Italy
    • Sacchi E, Tagliabue L, Duca F, Mannucci PM. High frequency of the C677T mutation in the methylenetetrahydrofolate reductase (MTHFR) gene in Northern Italy. Thromb Haemost 1997; 78: 963-4.
    • (1997) Thromb Haemost , vol.78 , pp. 963-964
    • Sacchi, E.1    Tagliabue, L.2    Duca, F.3    Mannucci, P.M.4
  • 8
    • 2342642866 scopus 로고    scopus 로고
    • Differences in the frequency of the C677T mutation in the methylenetetrahydrofolate reductase (MTHFR) gene among the Lebanese population
    • Almawi WY, Finan RR, Tamim H, Daccache JL, Irani-Hakime N. Differences in the frequency of the C677T mutation in the methylenetetrahydrofolate reductase (MTHFR) gene among the Lebanese population. Am J Hematol 2004; 76: 85-7.
    • (2004) Am J Hematol , vol.76 , pp. 85-87
    • Almawi, W.Y.1    Finan, R.R.2    Tamim, H.3    Daccache, J.L.4    Irani-Hakime, N.5
  • 9
    • 0033843870 scopus 로고    scopus 로고
    • The prevalence of factor V R506Q mutation-Leiden among apparently healthy Lebanese
    • Irani-Hakime N, Tamim H, Kreidy R, Almawi WY. The prevalence of factor V R506Q mutation-Leiden among apparently healthy Lebanese. Am J Hematol 2000; 65: 45-9.
    • (2000) Am J Hematol , vol.65 , pp. 45-49
    • Irani-Hakime, N.1    Tamim, H.2    Kreidy, R.3    Almawi, W.Y.4
  • 10
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    • Prevalence of factor V Leiden, prothrombin G20210A, and MTHFR C677T mutations in 200 healthy Jordanians
    • Eid SS, Rihani G. Prevalence of factor V Leiden, prothrombin G20210A, and MTHFR C677T mutations in 200 healthy Jordanians. Clin Lab Sci 2004; 17: 200-2.
    • (2004) Clin Lab Sci , vol.17 , pp. 200-202
    • Eid, S.S.1    Rihani, G.2
  • 11
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.