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Thromb Haemost 2004; 91(04): 832
DOI: 10.1055/s-0037-1614276
DOI: 10.1055/s-0037-1614276
Letters to the Editor
Reply to: A nucleic acid exchange in Intron F (Intron F-14T>G) in the human plasminogen gene is only a common polymorphism and not a true mutation
Weitere Informationen
Publikationsverlauf
Received
03. Oktober 2003
Accepted
12. November 2003
Publikationsdatum:
08. Dezember 2017 (online)
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References
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- 2 Bernardi F, Marchetti G, Pinotti M. et al.. Factor VII gene polymorphisms contribute about one third of the factor VII level variation in plasma. Arterioscler Thromb Vasc Biol 1996; 16: 72-6.
- 3 Perry DJ. Factor VII deficiency. Br J Haematol 2002; 118: 689-700.
- 4 Kanaji T, Okamura T, Osaki K. et al.. A common genetic polymorphism (46 C to T substitution) in the 5’-untranslated region of the coagulation factor XII gene is associated with low translation efficiency and decrease in plasma factor XII level. Blood 1998; 91: 2010-4.
- 5 Boncler MA, Golanski J, Paczuski R. et al.. Polymorphisms of glycoprotein Ib affect the inhibition by aurintricarboxylic acid of the von Willebrand factor dependent platelet aggregation. J Mol Med 2002; 80: 796-801.
- 6 Sartori MT, Vettor R, De Pergola G. et al.. Role of the 4G/5G polymorphismof PAI-1 gene promoter on PAI-1 levels in obese patients: influence of fat distribution and insulin-resistance. Thromb Haemost 2001; 86: 1161-9.