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Thromb Haemost 2002; 87(01): 170
DOI: 10.1055/s-0037-1612962
DOI: 10.1055/s-0037-1612962
Letters to the Editor
Absence of Mutations at the APC Interacting Sites of Factor VIII in Caucasians
Authors
Further Information
Publication History
Received
13 September 2001
Accepted
10 October 2001
Publication Date:
14 December 2017 (online)
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References
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- 2 Bertina RM, Koeleman BP, Koster T, Rosendaal FR, Dirven RJ, de Ronde H. et al. Mutation in blood coagulation factor V associated with resistance to activated protein C. Nature 1994; 369: 64-7.
- 3 Dahlbäck B, Carlsson M. Factor VIII defect associated with familial thrombophilia. Thrombosis and Haemostasis 1991; 65: 658A.
- 4 Dahlbäck B, Carlsson M, Svensson PJ. Familial thrombophilia due to a previously unrecognized mechanism characterized by poor anticoagulant response to activated protein C: prediction of a cofactor to activated protein C. Proc Natl Acad Sci USA 1993; 90: 1004-8.
- 5 Roelse JC, Koopman MM, Buller HR, ten Cate JW, Montaruli B, van Mourik JA. et al. Absence of mutations at the activated protein C cleavage sites of factor VIII in 125 patients with venous thrombosis. Br J Haematol 1996; 92: 740-3.
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- 7 Hooper WC, Dilley A, Austin H, Wenger NK, Benson J, Evatt BL. et al. Absence of mutations at APC cleavage sites Arg306 in factor V and Arg336, Arg562 in factor VIII in African-Americans. Thromb Haemost 1998; 79: 236.
- 8 Walker FJ, Scandella D, Fay PJ. Identification of the binding site for activated protein C on the light chain of factors V and VIII. J Biol Chem 1990; 265: 1484-9.
- 9 Bertina RM, Cupers R, van Wijngaarden A. Factor IXa protects activated factor VIII against inactivation by activated protein C. Biochem Biophys Res Commun 1984; 125: 177-83.