Absence of Prothrombin Mutation in Inuit (Greenland Eskimos)

• References

• 1 Bjerregaard P, Dyerberg J. Mortality from ischaemic heart disease and cerebrovascular disease in Greenland. Int J Epid 1988; 17: 514-9.
• 2 de Maat MPM, Jespersen J, Kluft C, Gram J. Absence of factor V Leiden mutation in Eskimos (Greenand Inuit). Lancet 1996; 347: 58-9.
• 3 de Maat MPM, Bladbjerg EM, Johansen LG, Bentzen J, Jespersen J. Pl^A1/A2 polymorphism of platelet glycoprotein IIIa and risk of cardiovascular disease. Lancet 1998; 349: 1099-100.
• 4 de Maat MPM, Green F, de Knijff P, Humphries S, Jespersen J, Kluft C. Factor VII polymorphisms in populations with different risk of cardiovascular disease. Arterioscl Thromb Vasc Biol 1997, In Press.
• 5 de Maat MPM, de Knijff P, Green FR, Thomas AE, Jespersen J, Kluft C. Gender-related association between ß-fibrinogen genotype and plasma fibrinogen levels and linkage disequilibrium at the fibrinogen locus in Greenland Inuit. Arterioscler Thromb Vasc Biol 1995; 15: 856-60.
• 6 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.
• 7 Cumming AM, Keeney S, Salden A, Bhavnani M, Shwe KH, Hay CRM. The prothrombin gene G20210A variant: prevalence in a U.K. anticoagulant clinic population. Br J Haem 1998; 98: 353-5.