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Thromb Haemost 1999; 81(06): 990
DOI: 10.1055/s-0037-1614612
DOI: 10.1055/s-0037-1614612
Letters to the Editor
Absence of the Prothrombin Gene Variant in Koreans
Further Information
Publication History
Received
31 December 1998
Accepted after revision
11 March 1999
Publication Date:
09 December 2017 (online)
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References
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- 3 Rosendaal FR, Siscovick DS, Schwartz SM, Psaty BM, Raghunathan TE, Vos HL. A common prothrombin variant (20210 G to A) increases the risk of myocardial infarction in young women. Blood 1997; 90: 1747-50.
- 4 Koelman BPC, Reitsma PH, Allaart CF, Bertina RM. Activated protein C resistance as an additional risk factor for thrombosis in protein C deficient families. Blood 1994; 84: 1031-4.
- 5 Song KS, Choi CR, Park Q, Lee A. Very low incidence of Arg506->Gln mutation in the factor V gene among Korean population. Thromb Haemost 1997. suppl 223
- 6 Kim YW, Yoon KY, Park S, Shim YS, Cho I H, Park SS. Absence of factor V Leiden mutation in Koreans. Thromb Res 1997; 86: 181-2.
- 7 Makris M, Preston FE, Beauchamp NJ, Cooper PC, Daly ME, Hampton KK, Bayliss P, Peake IR, Miller GJ. Co-inheritance of the 20210A allele of the prothrombin gene increases the risk of thrombosis in subjects with familial thrombophilia. Thromb Haemost 1997; 78: 1426-9.