References
- 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;88:3698–3703
- Gonzalez Ordonez AJ, Medina Rodriguez JM, Fernandez Alvarez CR, Macias Robles MD, Coto Garcia E. A patient homozygous for mutation 20210A in the prothrombin gene with venous thrombosis and transient ischemic attacks of thrombotic origin. Haematologica 1998;83:1050–1051
- Reddy P. Laboratory diagnosis of antiphospholipid syndrome. South Med J 2013;106:439–446
- Giannakopoulos B, Krilis SA. The pathogenesis of the antiphospholipid syndrome. N Engl J Med 2013;368:1033–1044
- Pretorius E, Lipinski B. Iron alters red blood cell morphology. Blood 2013;121:9
- Pretorius E. The adaptability of red blood cells. Cardiovasc Diabetol 2013;12:63--69