REFERENCES
- Wajcman H, Galactéros F. Hemoglobins with high oxygen affinity leading to erythrocytosis. New variants and new concepts. Hemoglobin. 2005;29(2):91–106.
- Agarwal N, Mojica-Henshaw MP, Simmons ED, Hussey D, Ou CN, Prchal JT. Familial polycythemia caused by a novel mutation in the β globin gene: essential role of P50 in evaluation of familial polycythemia. Int J Med Sci. 2007;4(4):232–236.
- Giardine B, van Baal S, Kaimakis P, et al. HbVar database of human hemoglobin variants and thalassemia mutations: 2007 update. Hum Mutat. 2007;28(2):206 (http://globin.cse.psu.edu).
- Percy MJ, Butt NN, Crotty GM, . Identification of high oxygen affinity hemoglobin variants in the investigation of patients with erythrocytosis. Haematologica. 2009;94(9):1321–1322.
- Miyazaki A, Nakanishi T, Shimizu A, Mizobuchi M, Yamada Y, Imai K. Hb Kochi [β141(H19)Leu→Val (g.1404 C→G); 144-146(HC1-3)Lys-Tyr-His→0 (g.1413 A→T)]: a new variant with increased oxygen affinity. Hemoglobin. 2005;29(1):1–10.
- Oliveira JL, Swanson K, Wendt P, Caughey TD, Hoyer JD. Hb Cambridge-MA [β144(HC1)-β146(HC3)Lys-Tyr-His→0 (HBB c.433 A>T)]: a new high oxygen affinity variant. Hemoglobin. 2010;34(6):565–571.
- Lorkin PA, Lehmann H, Fairbanks VF. The amino acid substitution in Hb Olmsted: β141 (H19) Leucine→Arginine. Biochim Biophys Acta. 1975;386(1):256–259.
- Aguilar-Martinez P, Badens C, Bonello-Palot N, et al. [Flowcharts for the diagnosis and the molecular characterization of hemoglobinopathies]. Ann Biol Clin (Paris). 2010;68(4):455–464.