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Hemoglobin
international journal for hemoglobin research
Volume 23, 1999 - Issue 3
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Original Article

Hb Harrow [β118(GH1)Phe→Cys]: A New Neutral Hemoglobin Variant

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Pages 273-279 | Received 17 Feb 1999, Accepted 07 Apr 1999, Published online: 07 Jul 2009

References

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  • 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 RatonFLUSA 1986; Vol. IV: 125–139
  • 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 (FGl)Hi→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
  • Hedlund B., Paine S., Smith C. M., II, Raines J., Morrison W. T., Adams J., III. Hemoglobin Minneapolis-Laos [β-118 (GH1) Phe→Tyr] a new hemoglobin variant with normal functional properties. Hemoglobin 1984; 8: 75–78
  • Steinberg M. H., Adams J. G., III, Morrison W. T., Pullen D. J., Abney R., Ibrahim A., Rieder R. F. Hemoglobin Mississipi (β44 ser→cys): studies of the thalassemic phenotype in a mixed heterozygote with β+-thalassemia. J. Clin. Invest. 1987; 79: 826–832

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