References
- Weatherall DJ, Clegg JB. Thalassemia—a global public health problem. Nat Med. 1996;2(8):847–849.
- Galanello R, Origa R. β-Thalassemia. Orphanet J Rare Dis. 2010;5:11.
- Cao A, Galanello R. β-Thalassemia. Genet Med. 2010;12(2):61–76.
- Cao A, Moi P, Galanello R. Recent advances in β-thalassemias. Pediatr Rep. 2011;3(2):e17.
- Giardine B, Borg J, Viennas E, et al. Updates of the HbVar database of human hemoglobin variants and thalassemia mutations. Nucleic Acids Res. 2014;16;42:(Database issue):D1063–D1069 (http://globin.cse.psu.edu).
- Murad H, Moasses F, Dabboul A, et al. Geographical distribution of β-globin gene mutations in Syria. Hematology. 2018;23(9):697–704.
- Yassin MM, Sirdah MM, Al Haddad RM, et al. Genotype-phenotype characteristics of β thalassemia children in the Gaza Strip, Palestine. J Genet Disor Genet Rep. 2013;2(2):1–6.
- Rujito L, Basalamah M, Siswandari W, et al. Modifying effect of XmnI, BCL11A, and HBS1L-MYB on clinical appearances: a study on β-thalassemia and Hemoglobin E/β-thalassemia patients in Indonesia. Hematol Oncol Stem Cell Ther. 2016;9(2):55–63.
- Tadmouri GO, Gulen RI. Deniz: the electronic database for β-thalassemia mutations in the Arab world. Saudi Med J. 2003;24(11):1192–1198.
- Indrak K, Brabec V, Indrakova J, et al. Molecular characterization of β-thalassemia in Czechoslovakia. Hum Genet. 1992;88(4):399–404.
- Villegas A, Ropero P, Gonzalez FA, et al. The thalassemia syndromes: molecular characterization in the Spanish population. Hemoglobin. 2001;25(3):273–283.
- Dobkin C, Pergolizzi RG, Bahre P, et al. Abnormal splice in a mutant human β-globin gene not at the site of a mutation. Proc Natl Acad Sci USA. 1983;80(5):1184–1188.
- Jiang F, Chen GL, Zhou JY, et al. First report of the rare IVS-II-705 (T>G) β-thalassemia mutation in a Chinese Family. Hemoglobin. 2017;41(4-6):286–287.
- Gilad O, Shemer OS, Dgany O, et al. Molecular diagnosis of β-thalassemia in a multiethnic population. Eur J Haematol. 2017;98(6):553–562.
- Zhang J, Yan J, Zeng F. Correction to: Recent progress on genetic diagnosis and therapy for β-thalassemia in China and around the world. Hum Gene Ther. 2018;29(3):400.
- Risoluti R, Materazzi S, Sorrentino F, et al. Update on thalassemia diagnosis: new insights and methods. Talanta. 2018;183:216–222.
- Asadov C, Alimirzoeva Z, Mammadova T, et al. β-Thalassemia intermedia: a comprehensive overview and novel approaches. Int J Hematol. 2018;108(1):5–21.
- Shahid S, Nadeem M, Zahid D, et al. α Thalassemia deletions found in suspected cases of β thalassemia major in Pakistani population. Pak J Med Sci. 2017;33(2):411–416.