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

The Hb Tarrant [α126(H9)Asp→Asn] Mutation is Localized in the α2-Globin Gene

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Pages 295-297 | Published online: 07 Jul 2009

References

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  • Moo-Penn W. F., Jue D. L., Johnson M. H., Wilson S. H., Therrell B., Schmidt R. M. Hemoglobin Tarrant: αl26(H9) Asp→Asn. A new hemoglobin variant in the α1β1 contact region showing high oxygen affinity and reduced cooperativity. Biochim. Biophys. Acta 1977; 490: 443–451
  • Ibarra B., Vaca G., Cantu J. M., Wilson J. B., Lam H., Stallings M., Gravely M. E., Huisman T. H. J. Heterozygosity and homozygosity for the high oxygen affinity Hemoglobin Tarrant or α126(H9)Asp→-Asn in two Mexican families. Hemoglobin 1982; 5: 337–348
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  • Dodé C., Rochette J., Krishnamoorthy R. Locus assignment of human α globin mutations by selective amplification and direct sequencing. Br. J. Haematol. 1990; 76: 275–281
  • Singer K., Chernoff A. I., Singer L. Studies on Abnormal Hemoglobins. I. Their demonstration in sickle cell anemia and other hematological disorders by means of alkali denaturation. Blood 1951; 6: 413–428

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