References
- Taher AT, Weatherall DJ, Cappellini MD. Thalassaemia. Lancet. 2018;391(10116):155–167.
- Giardine BM, Joly P, Pissard S, et al. Clinically relevant updates of the HbVar database of human hemoglobin variants and thalassemia mutations. Nucleic Acids Res. 2021;49(D1):D1192–D1196.
- Srivorakun H, Singha K, Fucharoen G, et al. Novel interactions of two α-Hb variants with SEA deletion α 0-thalassemia: hematological and molecular analyses. Hematology. 2018;23(3):187–191.
- Tuchinda S, Beale D, Lehmann H. A new haemoglobin in a Thai family. A case of Haemoglobin Siriraj-beta thalassaemia. Br Med J. 1965;1(5450):1583–1585.
- Guan Z-Y, Zhong Z-Y, He H-L, et al. Genetic counseling and prenatal decision for hemoglobin H disease caused by the rare α2 codon 30 (–GAG) (HBA2: c.91_93delGAG) mutation and the SEA deletion: case series study. Taiwan J Obstet Gynecol. 2021;60(4):763–765.
- Chang JG, Yang TY, Perng LI, et al. Hb Siriraj: a G→A substitution at codon 7 of the β-globin chain creates an MboII cutting site. Hemoglobin. 1999;23(2):197–199.
- Li Y, Huang T, Mao T, et al. Detection of a Hb A2-Melbourne (HBD: c.130G>A) combined with β-thalassemia in a Chinese individual. J Clin Lab Anal. 2020;34(9):e23401.
- Luo S, Chen X, Chen L, et al. Analysis of Hb levels and degree of anemia in relation to genotype in 615 patients with hemoglobin H disease. Expert Rev Hematol. 2020;13(9):1027–1033.
- Panyasai S, Kunyanone N, Satthakarn S. Hb Athens-Georgia (beta 40(C6) Arg>Lys, HBB:c.122G>A) with a single α-globin gene (Hb H disease) in a Thai family: molecular, hematological, and diagnostic aspects. Scand J Clin Lab Invest. 2021;81(1):52–58.
- Traivaree C, Boonyawat B, Monsereenusorn C, et al. Clinical and molecular genetic features of Hb H and AE Bart’s diseases in central Thai children. Appl Clin Genet. 2018;11:23–30.
- Chaibunruang A, Singha K, Srivorakun H, et al. Molecular characteristics of Hb New York [β113(G15)Val→Glu, HBB: c.341T>A] in Thailand. Hemoglobin. 2018;42(1):11–15.
- Satthakarn S, Panyasai S, Pornprasert S. Molecular Characterization of β- and α-globin gene mutations in individuals with borderline Hb A2 levels. Hemoglobin. 2020;44(5):349–353.