References
- Patrinos GP, Giardine B, Riemer C, et al. Improvements in the HbVar database of human hemoglobin variants and thalassemia mutations for population and sequence variation studies. Nucleic Acids Res. 2004;32(Database issue):D537–D541 (http://globin.cse.psu.edu/hbvar/menu.html)
- Oliveira JL, Swanson K, Wendt P, et al. Hb Cambridge-MA [β144(HC1)-β146(HC3)Lys-Tyr-His→0 (HBB: c.433 A>T)]: A new high oxygen affinity variant. Hemoglobin. 2010;34(6):565–571
- Konialis C, Hagnefelt B, Sevastidou S, et al. A novel β0-thalassemia frameshift mutation: [HBB: c.216delT]. Hemoglobin. 2012;36(6):586–588
- Angalena R, Aggarwal S, Phadke SR, Dalal A. Compound heterozygote condition in β thalassemia major due to a novel single nucleotide deletion (–T) at codon 69 in association with IVS 1-5 (G>C) mutation. Int J Lab Hematol. 2012;34(4):e7–e9
- Yu N, Kim HR, Cha YJ, Park EK. A novel frameshift mutation at codon 66 (HBB: c.del201A) in the β-globin gene leads to β-thalassemia. Ann Hematol. 2011;90:243–244