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Volumn 15, Issue 6, 2009, Pages 1342-1345

Clinical variability of haemophilia A and B in Mexican families by factor V Leiden G1691A, prothrombin G20210A and MTHFR C677T/A1298C

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE; BLOOD CLOTTING FACTOR 5 LEIDEN; BLOOD CLOTTING FACTOR 8; BLOOD CLOTTING FACTOR 9; CYTOSINE; GUANOSINE; METHYLENETETRAHYDROFOLIC ACID; PROTHROMBIN; THYMINE;

EID: 70449584734     PISSN: 13518216     EISSN: 13652516     Source Type: Journal    
DOI: 10.1111/j.1365-2516.2009.02069.x     Document Type: Letter
Times cited : (5)

References (11)
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  • 3
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    • The prothrombin 20210A allele influences clinical manifestations of haemophilia A in patients with intron 22 inversion and without inhibitors
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  • 4
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  • 6
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    • Pruthi, R.K.1    Heit, J.A.2    Green, M.M.3
  • 7
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  • 8
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  • 9
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    • A second common mutation in the methylenetetrahydrofolate reductase gene: an additional risk factor for neural-tube defects?
    • Van der Put NM, Gabreëls F, Stevens EM. A second common mutation in the methylenetetrahydrofolate reductase gene: an additional risk factor for neural-tube defects?. Am J Hum Genet 1998, 62:1044-51.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.