REFERENCES
- Harteveld CL, Higgs DR. α-Thalassaemia. Orphanet J Rare Dis. 2010;5(1):13.
- Traeger-Synodinos J, Douna V, Papassotiriou I, . Variable and often severe phenotypic expression in patients with the α-thalassemic variant Hb Agrinio [α29(B10)Leu→Pro (α2)]. Hemoglobin. 2010;34(5):430–438.
- de la Fuente-Gonzalo F, Vinuesa L, Martínez-Nieto J, . Recopilación de hemoglobinopatías de cadena α que cursan con microcitosis. Haematologica. 2010;95(2):44.
- Bernini LF, Harteveld CL. α Thalassaemia. Bailliéres’ Clin Haematol. 1998;11(1):53–90.
- Goossens M, Lee KY, Liebhaber SA, Kan YW. Globin structural mutant α125 Leu→Pro is a novel cause of α-thalassaemia. Nature. 1982;296(5860):864–865.
- Grové SS, Jenkins T, Kamuzora HL, Lehmann H. Congenital Heinz body haemolytic anaemia due to Hemoglobin Perth in a Nama child seemingly aggravated by the high nitrate content of the water supply. Act Haematol. 1977;57(3):143–151.
- Tanaka Y, Séller JF, Schwarta E, . Oxygen binding and stability properties of Hb Santa Ana (β88 LEU→PRO). Hemoglobin. 1985;9(2):157–169.
- Brennan SO, Shaw JC, George PM, Huisman THJ. Posttranslational modification of β141 Leu associated with the β75(E19)Leu→Pro mutation in the Hb Atlanta. Hemoglobin. 1993;17(1):1–7.
- Hall GW, Thein SL, Newland AC, . A base substitution (T→C) in codon 29 of the α2-globin gene causes α thalassaemia. Br J Haematol. 1993;85(3):546–552.
- Traeger-Synodinos J, Metaxotou-Mavromati A, Kanavakis E, . An α-thalassemic hemoglobinopathy: homozygosity for the Hb Agrinio α2-globin chain variant. Hemoglobin. 1998;22(3):209–215.
- Felekis X, Phylactides M, Drousiotou A, . Hb Agrinio [α29(B10)Leu→Pro (α2)] in combination with – –MED I results in a severe form of Hb H disease. Hemoglobin. 2008;32(3):237–246.
- de la Fuente-Gonzalo F, Vinuesa L, Martínez-Nieto J, . Biología Molecular de algunas hemoglobinas hiperinestables encontradas en la población española. Haematologica 2010;95(2):44.