References
- Weatherall DJ. Thalassemia as a global health problem: Recent progress toward its control in the developing countries. Ann N Y Acad Sci. 2010;1202:17–23
- Giardine B, Borg J, Viennas E, et al. Updates of the HbVar database of human hemoglobin variants and thalassemia mutations. Nucleic Acids Res. 2014;42(Database issue):D1063–D1069. ( http://globin.cse.psu.edu)
- Huang H, Xu L, Lin N, et al. A new β-thalassemia deletion mutation [codon 36 (–C)] observed in a Chinese woman. Hemoglobin. 2010;34(6):599–603
- Xu L, Huang H, Wang Y, et al. Molecular epidemiological analysis of α- and β-thalassemia in Fujian Province. Chinese J Med Genet. 2013;30(4):403–406
- Yang KG, Kutlar F, George E, et al. Molecular characterization of β-globin gene mutations in Malay patients with Hb E-β-thalassaemia and thalassaemia major. Br J Haematol. 1989;72(1):73–80
- Moradkhani K, Préhu C, Old J, et al. Mutations in the paralogous human α-globin genes yielding identical hemoglobin variants. Ann Hematol. 2009;88(6):535–543
- den Dunnen JT, Antonarakis SE. Mutation nomenclature extensions and suggestions to describe complex mutations: A discussion. Hum Mutat. 2000;15(1):7–12. [Erratum in: Hum Mutat. 2002;20(5):403]