References
- Bain BJ, Ed. Haemoglobinopathy Diagnosis, 2nd ed. Malden, MA: Blackwell Publishing Ltd. 2006:65–66
- Thein SL, Wallace RB, Pressley L, et al. The polyadenylation site mutation in the α-globin gene cluster. Blood. 1988;71(2):313–319
- Yüregir GT, Aksoy K, Cürük MA, et al. Hb H disease in a Turkish family resulting from the interaction of a deletional α-thalassaemia-1 and a newly discovered poly A mutation. Br J Haematol. 1992;80(4):527–532
- Hall GW, Higgs DR, Murphy P, et al. A mutation in the polyadenylation signal of the α2 globin gene (AATAAA→AATA– –) as a cause of α thalassaemia in Asian Indians. Br J Haematol. 1994;88(1):225–227
- Laosombat V, Fucharoen S, Wiriyasateinkul A. Interaction of the α2 polyadenylation signal mutation (AATAAA→AATA– –) and α0-thalassemia (– –SEA), resulting in Hb H disease in a Thai patient. Hemoglobin. 2001;25(4):383–389
- Nair SB, Nadkarni AH, Ghosh K, Colah RB. Variable presentation of Hb H disease due to homozygosity for the rare polyadenylation signal A TIndian (AATAAA > AATA– –) mutation in four Indian families. Hemoglobin. 2013;37(3):277–284
- Prior JF, Lim E, Lingam N, et al. A moderately severe α-thalassemia condition resulting from a combination of the α2 polyadenylation signal (AATAAA→AATA– –) mutation and a 3.7 kb α gene deletion in an Australian family. Hemoglobin. 2007;31(2):173–177
- Henderson S, Chapple M, Rugless M, et al. Haemoglobin H hydrops fetalis syndrome associated with homozygosity for the α2-globin gene polyadenylation signal mutation AATAAA→AATA– –. Br J Haematol. 2006;135(5):743–745
- Tan AS-C. A rapid and reliable 7-deletion multiplex polymerase chain reaction assay for α-thalassemia. Blood. 2001;98(1):250–251
- Steinberg MH, Forget BG, Higgs DR, Weatherall DJ, Eds. Disorders of Hemoglobin Genetics, Pathophysiology, and Clinical Management, 2nd ed. New York: Cambridge University Press, 2009
- Thein SL, Wallace RB, Pressley L, et al. The polyadenylation site mutation in the α-globin gene cluster. Blood. 1988;71(2):313–319
- Bhattacharya G, Sarkar AA, Banerjee D, et al. Polymerase chain reaction-based search for two α-globin gene mutations in India. Hemoglobin. 2008;32(5):485–490
- de Jong WW, Meera Khan P, Bernini LF. Hemoglobin Koya Dora: High frequency of a chain termination mutant. Am J Hum Genet. 1975;27(1):81–90
- Ho PJ, Rochette J, Rees DC, et al. Hb Sun Prairie: Diagnostic pitfalls in thalassemic hemoglobinopathies. Hemoglobin. 1996;20(2):103–112
- Plaseska D, Gu L-H, Wilson JB, et al. Hb Sun Prairie or α2130(H13)Ala→Proβ2; second observation in an Indian adult. Hemoglobin. 1990;14(5):491–497