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Thromb Haemost 2001; 85(05): 943-944
DOI: 10.1055/s-0037-1615777
DOI: 10.1055/s-0037-1615777
Letters to the Editor
A Novel Point Mutation in the 3’ Region of the Prothrombin Gene at Position 20221 in a Lebanese/Syrian Family
Weitere Informationen
Publikationsverlauf
Received
28. Dezember 2001
Accepted after resubmission
08. Januar 2001
Publikationsdatum:
11. Dezember 2017 (online)
M. W. and C. G. both contributed equally to this letter
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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 Oh J, Schaefer F, Veldmann A, Nowak G, Nowak-Gottl U, Tonshoff B, Kreuz W. Heterozygous prothrombin gene mutation: a new risk factor for early renal allograft thrombosis. Transplantation 1999; 68: 575-8.