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Volumn 109, Issue 1, 2003, Pages 71-72

Does the MTHFR 677T allele alter the clinical phenotype in severe haemophilia A?

Author keywords

Factor V Leiden; Haemophilia A; Methylene tetrahydrofolate reductase C677T; Prothrombin G20210A

Indexed keywords

ALLELE; BLEEDING; CLINICAL ARTICLE; CLINICAL TRIAL; CONTROLLED CLINICAL TRIAL; CONTROLLED STUDY; DISEASE SEVERITY; GENETIC ANALYSIS; GENETIC PROCEDURES; HEMOPHILIA A; HUMAN; INCIDENCE; LETTER; PHENOTYPE; PRIORITY JOURNAL;

EID: 0037241181     PISSN: 00493848     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0049-3848(03)00144-0     Document Type: Letter
Times cited : (19)

References (9)
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    • Escuriola Ettingshausen C., Halimeh S., Kurnik K., Schobess R., Wermes C., Junker R.et al. Symptomatic onset of severe hemophilia A in childhood is dependent on the presence of prothrombotic risk factors. Thromb. Haemost. 85(2):2001 (Feb.);218-220.
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  • 3
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    • Effect of the factor V Leiden mutation on the clinical expression of severe hemophilia A
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    • Lee D.H., Walker I.R., Teitel J., Poon M.C., Ritchie B., Akabutu J.et al. Effect of the factor V Leiden mutation on the clinical expression of severe hemophilia A. Thromb. Haemost. 83(3):2000 (Mar.);387-391.
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    • Lee, D.H.1    Walker, I.R.2    Teitel, J.3    Poon, M.C.4    Ritchie, B.5    Akabutu, J.6
  • 5
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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 S.R., Rosendaal F.R., Reitsma P.H., Bertina R.M. 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. 88:1996;3698-3703.
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  • 6
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    • (1994) Br. J. Haematol. , vol.88 , pp. 219-222
    • Beauchamp, N.1    Daly, M.2    Hampton, K.3    Cooper, P.4    Preston, F.5    Peake, I.6
  • 7
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    • A candidate genetic risk factor for vascular disease; A common mutation in methylenetetrahydrofolate reductase
    • Frosst P., Blom H.J., Minlos R., Goyette P., Sheppard C.A., Malhewes R.G.et al. A candidate genetic risk factor for vascular disease; a common mutation in methylenetetrahydrofolate reductase. Nat. Genet. 10:1995;111-113.
    • (1995) Nat. Genet. , vol.10 , pp. 111-113
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    • Arbini A.A., Mannucci P.M., Bauer K.A. Low prevalence of the factor V Leiden mutation among "severe" hemophiliacs with a "milder" bleeding diathesis. Thromb. Haemost. 74(5):1995 (Nov.);1255-1258.
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    • [accepted for publication]
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.