http://orcid.org/0000-0002-9827-7272
References
- Patrinos GP, Giardine B, Riemer C, et al. Improvements in the HbVar database of human hemoglobin variants and thalassemia mutations for population and sequence variation studies. Nucleic Acids Res. 2004;32(Database issue):D537–D541. (http://globin.cse.psu.edu)
- Little RR, Rohlfing CL, Hanson S, et al. Effects of hemoglobin (Hb) E and HbD traits on measurements of glycated Hb (HbA1c) by 23 methods. Clin Chem. 2008;54(8):1277–1282.
- Xu A, Sun J, Li J, et al. Hb I: a α-globin chain variant causing unexpected HbA1c results. J Clin Lab Anal. 2019;33(2):e22671
- Liang CC, Chen S, Yang K, et al. Hemoglobin Beijing [α16(A14)Lys→Asn]: a new fast-moving hemoglobin variant. Hemoglobin. 1982;6(6):629–633.
- Zeng YT, Huang SZ, Qiu XK, et al. Hemoglobin Chongqing [α2(NA2)Leu→Arg]. Hemoglobin. 1984;8(6):569–581.
- Lee YK, Kim HJ, Lee K, et al. Recent progress in laboratory diagnosis of thalassemia and hemoglobinopathy: a study by the Korean Red Blood Cell Disorder Working Party of the Korean Society of Hematology. Blood Res. 2019;54(1):17–22.
- Herpol M, Lanckmans K, Van Neyghem S, et al. Evaluation of the Sebia Capillarys 3 Tera and the Bio-Rad D-100 systems for the measurement of Hemoglobin A1c. Am J Clin Pathol. 2016;146(1):67–77.
- Chen WD, Ren YX, Wang YJ, et al. Compound heterozygosity for an unstable novel hemoglobin variant, Hb Dongguan [α52(E1)Ser→Cys (TCT>TGT); HBA1: c.158C>G], and the ––SEA (Southeast Asian) α-Thalassemia Deletion. Hemoglobin. 2019;43(4–5):286–288.
- Xu M, Chen WD, Wang YJ, et al. Hb Guangxi [β65(E9)Lys→Glu (AAG>GAG); HBB: c.196A>G]: a novel β-globin variant. Hemoglobin. 2019:1–2. doi:10.1080/03630269.2019.1653907
- Xu A, Chen W, Xia Y, et al. Effects of common hemoglobin variants on HbA1c measurements in China: results for α- and β-globin variants measured by six methods. Clin Chem Lab Med. 2018;56(8):1353–1361.