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Hemoglobin
international journal for hemoglobin research
Volume 24, 2000 - Issue 3
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Original Article

A New β-Globin Variant: Hb Sainte Eugénie [β104(G6)Arg→Trp] in a French Caucasian Female

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Pages 245-248 | Received 19 Nov 1999, Accepted 08 Feb 2000, Published online: 07 Jul 2009

References

  • Wilkinson T., Chua C. G., Carrell R. W., Robin H., Exner T., Lee K. M., Kronenberg H. A new haemoglobin variant, Haemoglobin Camperdown β104 (G6) Arginine→Serine. Biochim. Biophys. Acta 1975; 393: 195–200
  • Ryrie D. R., Plowman D., Lehmann H. Haemoglobin Sherwood Forest β104 (G6) Arg→Thr. FEBS Lett. 1977; 83: 260–262
  • Prome D., Prome J. C., Deon C., Groff P., Kalmes G., Galacteros F., Wajcman H. Structural determination of a new electrophoreticaly silent variant: Hemoglobin Alzette, β104(G6)Arg→Lys. Rapid Commun. Mass Spectrom. Spec, N˚. 1995; S165–8
  • Alter B. P., Goff S. C., Efremov G. D., Gravely M. E., Huisman T. H.J. Globin chain electrophoresis: a new approach to the determination of the Gγ/Aγ ratio in fetal haemoglobin and to studies of globin synthesis. Br. J. Haematol. 1980; 44: 527–534
  • Lacan P., Kister J., Francina A., Souillet G., Galactéros F., Delaunay J., Wajcman H. Hemoglobin Debrousse [β96(FG3) Leu→Pro]: a new unstable hemoglobin with twofold increased oxygen affinity. Am. J. Hematol. 1996; 51: 276–281
  • Morlé F., Francina A., Ducrocq R., Wajcman H., Gonnet C., Philippe N., Souillet G., Godet J. A new α chain variant Hb Sallanches [α2 104(G11) Cys→Tyr] associated with Hb H disease in one homozygous patient. Br. J. Haematol. 1995; 91: 608–611
  • Williamson D., Perry D. J., Brown K., Langdown J. V. Compound heterozygosity for two β chain variants: Hb S [β6(A3)Glu→Val] and the high affinity variant Hb San Diego [β109(G11)Val→Met]. Hemoglobin 1995; 19: 27–32
  • Kister J., Poyart C., Edelstein S. J. An expanded two-state allosteric model for interactions of human Hemoglobin A with nonsaturating concentrations of 2,3-diphosphoglycerate. J. Biol. Chem. 1987; 262: 12085–12091
  • Jelkmann W., Bauer C. What is the best method to remove 2,3-diphosphoglycerate from hemoglobin? Anal. Biochem. 1976; 75: 382–388

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