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Thromb Haemost 1998; 80(01): 201-202
DOI: 10.1055/s-0037-1615165
DOI: 10.1055/s-0037-1615165
Letters to the Editor
Recurrent Thromboembolism in Two Unrelated Patients with Double Heterozygosity for Factor V R506Q and Factor II 20210G/A Mutations
Further Information
Publication History
Received
29 January 1998
Accepted after revision
23 March 1998
Publication Date:
08 December 2017 (online)

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References
- 1 Poort SR, Rosendaal FR, Reitsma PH, Bertina RM. 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 1996; 88: 3698-703.
- 2 Hillarp A, Zöller B, Svensson PJ. Dahlbäck. The 20210 A allele of the prothrombin gene is a common risk factor among Swedish outpatients with verified deep venous thrombosis.. Thromb Haemost 1998; 78: 990-2.
- 3 Brown K, Luddington R, Williamson D, Baker P, Baglin T. Risk of venous thromboembolism associated with a G to A transition at position 20210 in the 3’-untranslated region of the prothrombin gene.. Br J Haematol 1998; 98: 907-9.
- 4 Bertina RM, Koeleman BPC, Koster T, Rosendaal FR, Dirven RJ, de Ronde H, Van der Velden PA, Reitsma PH. Mutation in blood coagulation factor V associated with resistance to activated protein C.. Nature 1994; 369: 64-7.
- 5 Alhenc-Gelas M, Le Cam-Duchez V, Emmerich J, Frebourg T, Fiessinger JN, Borg JY, Aiach M. The A 20210 allele of the prothrombin gene is not frequently associated with the factor V Arg 506 to Gln mutation in thrombophilic families.. Blood 1998; 90: 1711.