References
- Huisman T. H.J., Wilson J. B., Kutlar A., Yang K. G., Chen S. S., Webber B. B., Altay Č., Martinez Villegas A. Hb J-Antakya or α2β2 65(E9) Lys→Met in a Turkish family and Hb Complutense or α2β2 127(H5) Gln→Glu in a Spanish family; correction of a previously published identification. Biochim. Biophys. Acta 1986; 871: 229–231
- Huisman T. H.J., Carver M. F.H., Efremov G. D. A Syllabus of Human Hemoglobin Variants Second Edition. The Sickle Cell Anemia Foundation, Augusta, GAUSA 1998, http://globin.cse.psu.edu
- Hocking D. R. The Separation and Identification of Hemoglobin Variants by Isoelectric Focusing Electrophoresis: an Interpretive Guide, T. H.J. Huisman. Isolab Inc., Akron, OHUSA 1997
- Schneider R. G., Barwick R. C. Electrophoretic mobilities of mutant hemoglobins and mutant globin chains. CRC Handbook Series in Clinical Laboratory Science, Section I: Hematology, R. M. Schmidt, V. F. Fairbanks. CRC Press, Boca Raton, FLUSA 1986; Vol. IV: 125–139
- Riou J., Godart C., Hurtrel D., Mathis M., Bimet C., Bardakdjian-Michau J., Préhu C., Wajcman H., Galactéros F. Evaluation of cation-exchange high-performance liquid-chromatography for presumptive identification of hemoglobin variants. J. Clin. Chem. 1997; 43: 34–39
- Wajcman H., Bardakdjian J., Ducrocq R. Structural characterization of abnormal hemoglobins from dried blood specimens in a neonatal screening program. Ann. Biol. Clin. 1993; 50: 867–870
- Déon C., Promé J. C., Promé D., Francina A., Groff P., Kalmes G., Galactéros F., Wajcman H. Combining mass spectrometry methods allows characterization of human hemoglobin variants localized within αT9 peptide: identification of Hb Villeurbanne α89 (FG1) His→Tyr. J. Mass Spectrom. 1997; 32: 880–887
- Kister J., Poyart C., Edelstein S. J. An expanded two-state allosteric model for interaction of human Hemoglobin A with non saturating concentrations of 2,3 diphosphoglycerate. J. Biol. Chem. 1987; 262: 12085–12091
- Wajcman H., Blouquit Y., Vasseur C., Le Querrec A., Laniece M., Melevendi C., Rasore A., Galactéros F. Two new human hemoglobin variants caused by unusual mutational events: Hb ZaTre that contains a five residue repetition within the α-chain and Hb Duino has two residues substituted in the β-chain. Hum. Genet. 1992; 78: 676–680
- Lacombe C., Craescu C. T., Blouquit Y., Kister J., Poyart C., Delanoe-Garin J., Arous N., Bardakdjian J., Riou J., Rosa J., Schaeffer C., Galactéros F. Structural and functional studies of Hemoglobin Poissy α2β2 56(D7) Gly→Arg and 86 (F2) Ala→Pro. Eur. J. Biochem. 1985; 153: 655–662
- van den Berg H. M., Bruin M. C.A., Batelaan D., van Delft P., van Zwieten R., Roos D., Harteveld C. L., Bernini L. F., Giordano P. C. Hb Nijkerk: a new mutation at codons 138/139 of the β-globin gene inducing severe hemolytic anemia in a Dutch girl. Hemoglobin 1999; 23: 135–144
- Lacombe C., Promé D., Blouquit Y., Bardakdjian J., Arous N., Mrad A., Promé J C., Rosa J. New results of hemoglobin variant structure determinations by fast atom bombardment mass spectrometry. Hemoglobin 1990; 14: 529–548
- Préhu C., Bost M., Barro C., Promé D., Riou J., Godart C., Kister J., Galactéros F., Wajcman H. Hb Roubaix [α55(E4)Val→Leu]: a new neutral hemoglobin variant involving the α1 gene. Hemoglobin 1999; 24: 361–365