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Volumn 2, Issue 2, 2004, Pages 361-362

The prevalence of factor V G1691A but not of prothrombin G20210A and methylenetetrahydrofolate reductase C677T is remarkably low in French Basques [9]

Author keywords

[No Author keywords available]

Indexed keywords

5,10 METHYLENETETRAHYDROFOLATE REDUCTASE (FADH2); BLOOD CLOTTING FACTOR 5; BLOOD CLOTTING FACTOR 5 LEIDEN; PROTHROMBIN; METHYLENETETRAHYDROFOLATE REDUCTASE (NADPH2);

EID: 4644227898     PISSN: 15387933     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1538-7933.2004.0584i.x     Document Type: Letter
Times cited : (11)

References (13)
  • 3
    • 0030476647 scopus 로고    scopus 로고
    • The population genetics of factor V Leiden (Arg506Gln)
    • Rees DC. The population genetics of factor V Leiden (Arg506Gln). Br J Haematol 1996; 95: 579-86.
    • (1996) Br. J. Haematol. , vol.95 , pp. 579-586
    • Rees, D.C.1
  • 5
    • 0034849561 scopus 로고    scopus 로고
    • Genetic risk factors for thrombosis in a Basque population and their possible contribution to the analysis of a complex disease such as thrombophilia
    • [letter]
    • Soria JM, Baiget M, Castano L, Tejada MI, Peretz-Nanclares G. Genetic risk factors for thrombosis in a Basque population and their possible contribution to the analysis of a complex disease such as thrombophilia. Haematologica 2001; 86: 889-90 [letter].
    • (2001) Haematologica , vol.86 , pp. 889-890
    • Soria, J.M.1    Baiget, M.2    Castano, L.3    Tejada, M.I.4    Peretz-Nanclares, G.5
  • 6
    • 0000449738 scopus 로고    scopus 로고
    • Frequency of factor V Leiden (Arg506Gln) in France
    • Lucotte G, Mercier G. Frequency of factor V Leiden (Arg506Gln) in France. Br J Haematol 1997; 99: 237-41.
    • (1997) Br. J. Haematol. , vol.99 , pp. 237-241
    • Lucotte, G.1    Mercier, G.2
  • 7
    • 0035912152 scopus 로고    scopus 로고
    • Genetic susceptibility to venous thrombosis
    • Seligsohn U, Lubetsky A. Genetic susceptibility to venous thrombosis. N Engl J Med 2001; 344: 1222-31.
    • (2001) N. Engl. J. Med. , vol.344 , pp. 1222-1231
    • Seligsohn, U.1    Lubetsky, A.2
  • 8
    • 0034190659 scopus 로고    scopus 로고
    • 5,10-Methylenetetrahydrofolate reductase gene variants and congenital anomalies: A huge review
    • Botto LD, Yang Q. 5,10-Methylenetetrahydrofolate reductase gene variants and congenital anomalies: a huge review. Am J Epidemiol 2000; 151: 862-77.
    • (2000) Am. J. Epidemiol. , vol.151 , pp. 862-877
    • Botto, L.D.1    Yang, Q.2
  • 11
    • 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


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.