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Thromb Haemost 1998; 80(06): 1028-1029
DOI: 10.1055/s-0037-1615407
DOI: 10.1055/s-0037-1615407
Letters to the Editor
Homozygous G20210A Prothrombin Gene Mutation without Thromboembolic Events: A Case Report
Further Information
Publication History
Received
19 May 1998
Accepted after revision
01 September 1998
Publication Date:
07 December 2017 (online)
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References
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- 2 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.
- 3 Doggen CJM, Manger Cats V, Bertina RM, Rosendaal FR. Interaction of coagulation defects and cardiovascular risk factors: increased risk of myocardial infarction associated with factor V Leiden or prothrombin 20210A. Circulation 1998. (in press).
- 4 Kapur RK, Mills LA, Spitzer SG, Hultin MB. A prothrombin gene mutation is significantly associated with venous thrombosis. Arterioscler Thromb Vasc Biol 1997; 17: 2875-9.
- 5 Howard TE, Marusa M, Channell C, Duncan A. A patient homozygous for a mutation in the prothrombin gene 3’-untranslated region associated with massive thrombosis. Blood Coag Fibrinol 1997; 8: 316-9.
- 6 Scott CM, Hanley JP, Ludlam CA, Stirling D. Homozygosity for a factor II polymorphism associated with thrombosis during pregnancy. Thromb Haemost. 1997 (Suppl.)770 (Abstract).