REFERENCES
- Weatherall D. Beginnings: the molecular pathology of hemoglobin. Molecular Hematology, 2nd, D Provan, JG Gribben. Blackwell Publishing, Malden 2005; 1–17
- Kazazian HH, Jr. The thalassemia syndromes: molecular basis and prenatal diagnosis in 1990. Semin Hematol 1990; 27(3)209–228
- Ohba Y, Hattori Y, Harano T, Harano K, Fukumaki Y, Ideguchi H. β-Thalassemia mutations in Japanese and Koreans. Hemoglobin 1997; 21(2)191–200
- Viprakasit V, Chinchang W, Suwanthol L, Tanphaichitr VS. Common origin of a rare β-globin initiation codon mutation (ATG→AGG) in Asians. Clin Lab Hematol 2005; 27(6)409–415
- Rund D, Rachmilewitz E. β-Thalassemia. N Engl J Med 2005; 353(11)1135–1146
- Waye JS, Eng B, Patterson M, Barr RD, Chui DHK. De novo mutation of the β-globin initiation codon (ATG→AAG) in a Northern European boy. Am J Hematol 1997; 56(3)179–182