References
- Lahiry P, Al-Attar SA, Hegele RA. Understanding β-thalassemia with focus on the Indian Subcontinent and the Middle East. Open Hematol J. 2008;2:5–13
- Gonzalez-Redondo JM, Stoming TA, Lanclos KD, et al. Clinical and genetic heterogeneity in Black patients with homozygous β-thalassemia from the southeastern United States. Blood. 1988;72(3):1007–1014
- Goldsmith ME, Humphries RK, Ley T, et al. Silent substitution in β-thalassemia gene activating a cryptic splice site in β-globin RNA coding sequence. Proc Natl Acad Sci USA. 1983;80(8):2318–2322
- Old J. Haemoglobinopathies. Prenat Diagn. 1996;16(13):1181–1186
- Agouti I, Bennani M, Levy N, et al. The rare codon 24 (A > T) (β+) mutation in association with the common codon 39 (C > T) (β0) mutation causes transfusion-dependent β-thalassemia in a Moroccan patient. Hemoglobin. 2009;33(2):150–154
- Veten FM, Abdelhamid I, Meiloud G, et al. Hb S [β6(A3)Glu→Val, GAG > GTG] and β-globin gene cluster haplotype distribution in Mauritania. Hemoglobin. 2012;36(4):311–315
- Hamed CT, Bollahi MA, Abdelhamid I, et al. Frequencies and ethnic distribution of ABO and Rh(D) blood groups in Mauritania: Results of first nationwide study. Int J Immunogenet. 2012;39(2):151–154
- Gonzalez-Redondo, JM, Kutlar A, Kultar F, et al. Molecular characterizationof Hb S(C) β-thalassemia in American Blacks. Am J Hematol. 1991;38(1):9–14
- Hattori Y, Yamane A, Yamashiro Y, et al. Characterization of β-thalassemia mutations among Japanese. Hemoglobin. 1989;13(7):657–670