https://orcid.org/0000-0002-8640-7375
References
- 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.
- Lin M, Wang Q, Zheng L, et al. Prevalence and molecular characterization of abnormal hemoglobin in eastern Guangdong of southern China. Clin Genet. 2012;81(2):165–171.
- Liu Y-N, Li R, Zhou J-Y, et al. Screening for mutations in the a-globin genes leading to abnormal hemoglobin variants with high resolution melting analysis. Clin Chem Lab Med. 2011;50(2):273–277.
- Li Y-Q, Huang H-P, Chen Z-Z, et al. Comparison of capillary electrophoresis and high performance liquid chromatography for detection and quantification of hemoglobin New York. Clin Chem Lab Med. 2016;54(1):91–95.
- Munkongdee T, Chen P, Winichagoon P, et al. Update in laboratory diagnosis of thalassemia. Front Mol Biosci. 2020;7:74.
- Srivorakun H, Fucharoen G, Sanchaisuriya K, et al. Diagnosis of common hemoglobinopathies among South East Asian population using capillary isoelectric focusing system. Int J Lab Hematol. 2017;39(1):101–111.
- Zhao Y-L, Lin Q-F, He X-W, et al. Hb Hezhou [β64(E8)Gly→Ser; HBB: c.193G>A]: a novel variant on the β-globin gene. Hemoglobin. 2021;45(2):133–135.
- Pondman KM, Brinkman JW, van der Straaten HM, et al. Hb Nouakchott [α114(GH2)Pro→Leu; HBA1: c.344C>T], a second and third case described in two unrelated Dutch families. Hemoglobin. 2018;42(1):51–53.
- Kountouris P, Lederer CW, Fanis P, et al. IthaGenes: an interactive database for haemoglobin variations and epidemiology. PLOS One. 2014;9(7):e103020.
- Bisconte MG, Caldora M, Musollino G, et al. α-Thalassemia associated with hb instability: a tale of two features. The case of Hb Rogliano or α1 Cod 108(G15)Thr→Asn and Hb Policoro or α2 Cod 124(H7)Ser→Pro. PLOS One. 2015;10(3):e0115738.