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.