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Thromb Haemost 1998; 80(04): 705-706
DOI: 10.1055/s-0037-1615448
DOI: 10.1055/s-0037-1615448
Letters to the Editor
A Polymorphism nt 1628G→A (R485K) in Exon 10 of the Coagulation Factor V Gene May Be a Risk Factor for Thrombosis in the Indigenous Thai Population
Weitere Informationen
Publikationsverlauf
Received
15. April 1998
Accepted after revision
18. Juni 1998
Publikationsdatum:
08. Dezember 2017 (online)
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References
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- 3 Ishida F, Ito T, Ichikawa N, Shimodaira S, Takamiya O, Furihata K, Kiyosawa K, Kitano K. Arg506Gln factor V mutation is uncommon in Eastern Asian populations. Blood 1995; 86: 917a.
- 4 Sifontes MT, Nuss R, Hunger SP, Wilimas J, Jacobson LJ, Manco-Johnson MJ. The factor V Leiden mutation in children with cancer and thrombosis. Br J Haematol 1997; 96: 484-9.
- 5 Gandrille S, Greengard JS, Alhenc-Gelas M, Juhan-Vague I, Abgrall JF, Jude B, Griffin JH, Aiach M. the French Network on behalf of INSERM. Incidence of activated protein C resistance caused by the Arg 506 Gln mutation on factor V in 113 unrelated symptomatic protein C deficient patients. Blood 1995; 86: 219-24.
- 6 Helley D, Besmond C, Ducrocq R, da Silva F, Guillin M-C, Bezeaud A, Elion J. Polymorphism in exon 10 of the human coagulation factor V gene in a population at risk for sickle cell disease. Hum Genet 1997; 100: 245-8.
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