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Thromb Haemost 1999; 82(03): 1197-1198
DOI: 10.1055/s-0037-1614353
DOI: 10.1055/s-0037-1614353
Letters to the Editor
Lack of Association between Hemochromatosis and Factor V Leiden Mutations in the Czech Population
Weitere Informationen
Publikationsverlauf
Received
29. März 1999
Accepted after revision
20. April 1999
Publikationsdatum:
09. Dezember 2017 (online)
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References
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- 3 Bertina RM, Koeleman BP, 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.
- 4 Lynas C. A cheaper and more rapid polymerase chain reaction-restriction fragment length polymorphism method for the detection of the HLA-H gene mutation occurring in hereditary hemochromatosis. Blood 1997; 90: 4235-6.
- 5 Tordai A, Andrikovics H, Kalmár L, Rajczy K, Pénzes M, Sarkadi B, Klein I, Váradi A. High frequency of the haemochromatosis C282Y mutation in Hungary could argue against a Celtic origin of the mutation. J Med Genet 1998; 35: 878-9.
- 6 Nielsen P, Carpinteiro S, Fischer R, Cabeda JM, Porto G, Gabbe EE. Prevalence of the C282Y and H63D mutations in the HFE gene in patients with hereditary haemochromatosis and in control subjects from Northern Germany. Br J Haematol 1998; 103: 842-5.