The frequency of factor V Leiden and prothrombin G20210A mutations in Slovak and Roma (Gypsy) ethnic group of Eastern Slovakia-Reference-Cited by-同舟云学术

The frequency of factor V Leiden and prothrombin G20210A mutations in Slovak and Roma (Gypsy) ethnic group of Eastern Slovakia

Published:2012-05-05 Issue:3 Volume:34 Page:406-409
ISSN:0929-5305
Container-title:Journal of Thrombosis and Thrombolysis
language:en
Short-container-title:J Thromb Thrombolysis

Author:

Bôžiková Alexandra,Gabriková Dana,Sovičová Adriana,Behulová Regina,Mačeková Soňa,Boroňová Iveta,Petrejčíková Eva,Soták Miroslav,Bernasovská Jarmila,Bernasovský Ivan

Publisher

Springer Science and Business Media LLC

Subject

Cardiology and Cardiovascular Medicine,Hematology

Link

http://link.springer.com/content/pdf/10.1007/s11239-012-0736-4.pdf

Reference34 articles.

1. Rosendaal FR (1997) Thrombosis in the young: epidemiology and risk factors: a focus on venous thrombosis. Thromb Haemost 78(1):1–6

2. Bertina RM, Koeleman BPC, Koster T et al (1994) Mutation in blood coagulation factor V associated with resistance to activated protein C. Nature 369(6475):64–67. doi: 10.1038/369064a0

3. Zivelin A, Griffin JH, Xu X et al (1997) A single genetic origin for a common Caucasian risk factor for venous thrombosis. Blood 89:397–402

4. Rees DC, Cox M, Clegg JB (1995) World distribution of factor V Leiden. Lancet 346:1133–1134

5. Irani-Hakime N, Tamim H, Kreidy R et al (2000) The prevalence of factor V R506Q mutation-Leiden among apparently healthy lebanese. Am J Hematol 65(1):45–49. doi: 10.1002/1096-8652(200009)65:1<45:AID-AJH8>3.0.CO;2-V

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