A Rare ?°-Thalassemia Frameshift Mutation in a Turkish Individual: (+T) at Codon 9/10

Kaynakça (2)

1. Weatherall DJ, Clegg JB. The thalassemia syndromes. Oxford: Black- well Sciences, 2001. [CrossRef] Angastiniotis M, Modell B. Global epidemiology of hemoglobin disor- ders. Ann NY Acad Sci 1998; 850: 251-69. [CrossRef] Altay C. The frequency and distribution pattern of ?-thalassemia mu- tations in Turkey. Turkish J Hematol 2002; 19(2): 309-15.
2. Akhavan-Niaki H, Derakhshandeh-Peykar P, Banihashemi A, Mosta- fazadeh A, Asghari B, Ahmadifard MR, et al. A comprehensive mol- eculer characterization of beta thalassemia in a highly heterogeneous population. Blood Cells Mol Dis 2011; 47(1): 29-32. [CrossRef] Akar N, Cavdar AO, Dessi E, Loi A, Pirastu M, Cao A. Beta thal- assaemia mutations in Turkish population. J Med Genet 1987; 24(6): 378-9. [CrossRef] Basak AN. The Molecular pathology of beta-thalassemia in Turkey: The Boğazıcı University experience. Hemoglobin 2007; 31(2): 233- 41. [CrossRef] Waye JS, Eng B, Oliveri NF, Chui DH. Identification of a novel beta O-thalassaemia mutation in a Greek family and subsequent prenatal diagnosis. Prenatal Diag 1994; 14(10): 929-32. [CrossRef] Rahimi Z, Muniz A, Parsian A. Detection of responsible mutations for beta thalassemia in the Kermanshah Province of Iran using PCR- based techniques. Mol Biol Rep 2010; 37(1): 149-50. [CrossRef] Gunesacar R, Celik MM. First report from Turkey of a rare frameshift mutation [codons 9/10 (+T)] in the beta-globin gene. Turk J Hematol 2011; 28: 343-5. [CrossRef] Filon D, Oron V, Shawa R, Elborno E, Najjar K, Tulchinsky T, et al. Spectrum of beta-thalassemia mutations in the Gaza area. Hum Mutat 1995; 5(4): 351-3. [CrossRef] Giardine B, van Baal S, Kaimakis P, Riemer C, Miller W, Samara M, et al. HbVar database of human hemoglobin variants and thalassemia mutations: 2007 update. Hum Mutat 2007; 28(2): 206. [CrossRef]