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Hemoglobin
international journal for hemoglobin research
Volume 37, 2013 - Issue 2
105
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Short Communication

Microdeletion Of Exon 3 In The HBA2 Gene Associated With Mild α-Thalassemia Trait

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Pages 192-196 | Received 27 Sep 2012, Accepted 19 Nov 2012, Published online: 29 Jan 2013

REFERENCES

  • Harteveld CL, Higgs DR. α-Thalassaemia. Orphanet J Rare Dis. 2010;5:13.
  • Higgs DR. The molecular basis of α thalassemia. In: Steinberg MH, Forget BG, Higgs DR, Weatherall DJ, Eds. Disorders of Hemoglobin: Genetics, Pathophysiology, and Clinical Management, 2nd ed. Cambridge: Cambridge University Press. 2009:241–265.
  • Au NHC, Wong AYK, Vickars L, MacGillivray RTA, Wadsworth LD. Two new examples of Hb St. Etienne [β92(F8)His→Gln] in association with venous thrombosis. Hemoglobin. 2009;33(2):95–100.
  • Twomey AP, Brasch JM, Betheras FR, Bowden DK. A new α2-globin gene [codon 90 (AAG→TAG)] nonsense mutation. Hemoglobin. 2003;27(4):261–265.
  • Liebhaber SA, Coleman MB, Adams JG 3rd. Cash FE, Steinberg MH. Molecular basis for nondeletion α-thalassemia in American blacks. α2(116GAG→UAG). J Clin Invest. 1987;80(1):154–159.

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