REFERENCES
- Patrinos GP, Giardine B, Riemer C, et al. Improvements in the HbVar database of human hemoglobin variants and thalassemia mutations for population and sequence variation studies. Nucleic Acids Res. 2004;32(Database issue):D537-D541 (http://globin.cse.psu.edu).
- Wajcman H, Galacteros F. Hemoglobins with high oxygen affinity leading to erythrocytosis. New variants and new concepts. Hemoglobin. 2005;29(2):91–106.
- Blouquit Y, Delanoe-Garin J, Lacombe C, Structural study of Hemoglobin Hazebrouck, β38(C4)Thr→Pro. A new abnormal hemoglobin with instability and low oxygen affinity. FEBS Lett. 1984;172(2):155–158.
- Ropero P, Fernandez-Lago C, Villegas A, Hb La Coruna [β38(C4)Thr→Ile]: a new hemoglobin variant leading to familial polycythemia. Hemoglobin. 2006:30(3):379–383.
- Cuccia L, Saieva L, Borsellino Z, Hb Hinwil [β38(C4)Thr→Asn, ACC>AAC] associated with β0-thalassemia in a Sicilian child. Hemoglobin. 2008;32(6):582–587.
- Frischknecht H, Ventruto M, Hess D, Hb Hinwil or β38(C4)Thr→Asn: a new β chain variant detected in a Swiss family. Hemoglobin. 1996;20(1):31–40.
- Winslow RM, Swenberg ML, Berger RL, Oxygen equilibrium curve of normal human blood and its evaluation by Adair’s equation. J Biol Chem. 1977;252(7):2331–2337.
- Schneider RG, Barwick RC. Measuring relative electrophoretic mobilities of mutant hemoglobins and globin chains. Hemoglobin 1978:2(5):417–435.
- Sack JS, Andrews LC, Magnus KA, Hanson JC, Rubin J, Love WE. Location of amino acid residues in human deoxy hemoglobin. Hemoglobin. 1978;2(2):153–169.