References
- Christopher AF, Kumari A, Chaudhary S, et al. Unique pattern of mutations in β-thalassaemia patients in Western Uttar Pradesh. Indian J Hum Genet. 2013;19(2):207–212
- Mentzer WC, Kan YW. Prospects for research in hematologic disorders: Sickle cell disease and thalassemia. JAMA. 2001;285(5):640–642
- Kumar R, Singh K, Panigrahi I, Agarwal S. Genetic heterogeneity of β-globin mutations among Asian-Indians and importance in genetic counselling and diagnosis. Mediterr J Hematol Infect Dis. 2013;5(1):e2013003. doi: 10.4084/MJHID.2013.003
- Elmezayen AD, Kotb SM, Sadek NA, Abdalla EM. β-Globin mutations in Egyptian patients with β-thalassemia. Lab Med. 2015;46(1):8–13
- Akhavan-Niaki H, Seresti SS, Asghari B, Banihashemi A. IVSII-666 of human β-globin gene: A polymorphic marker linked to codon 8(–AA) mutation. Genet Test Mol Biomarkers. 2011;15(7–8):573–576
- Habibzadeh F, Yadollahie M, Merat A, Haghshenas H. Thalassemia in Iran; an overview. Arch Iran Med. 1998;1(1):27–34
- Akhavan-Niaki H, Derakhshandeh-Peykar P, Banihashemi A, et al. A comprehensive molecular characterization of β thalassemia in a highly heterogeneous population. Blood Cells Mol Dis. 2011;47(1):29–32
- Derakhshandeh-Peykar P, Akhavan-Niaki H, Tamaddoni A, et al. Distribution of β-thalassemia mutations in the northern provinces of Iran. Hemoglobin. 2007;31(3):351–356
- Landin B, Berglund S. A novel mutation in the β-globin gene causing β-thalassaemia in a Swedish family. Eur J Haematol. 1996;57(2):182–184
- Nasouhipur H, Banihashemi A, Youssefi Kamangar R, Akhavan-Niaki H. Hb Knossos: HBB:c.82G > T associated with HBB:c.315 + 1G > A β0 mutation causes thalassaemia intermedia. Indian J Hematol Blood Transfus. 2014;30(Suppl 1):243–245
- 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)