References
- Lacan P, Aubry M, Couprie N, et al. Two new α chain variants: Hb Die [α93(FG5)Val→Ala (α1)] and Hb Beziers [α99(G6)Lys→Asn (α1)]. Hemoglobin. 2004;28(1):59–63.
- Lacerra G, Testa R, De Angioletti M, et al. Hb Bronte or α93(FG5)Val→Gly: a new unstable variant of the α2-globin gene, associated with a mild α+-thalassemia phenotype. Hemoglobin. 2003;27(3):149–159.
- Ohba Y. Unstable hemoglobins. Hemoglobin. 1990;14(4):353–388.
- Cepreganova B, Wilson JB, Huisman THJ, et al. Hb Nottingham or α2β298(FG5)Val→Gly observed as a de novo mutation in a Canadian child. Hemoglobin. 1992;16(1-2):77–79.
- Gacon G, Wajcman H, Labie D, et al. A new unstable hemoglobin mutated in β98 (FG5)Val leads to Ala: Hb Djelfa. FEBS Lett. 1975;58(1–2):238–240.
- Kleinert P, Schmid M, Zurbriggen K, et al. Mass spectrometry: a tool for enhanced detection of hemoglobin variants. Clin Chem. 2008;54(1):69–76.
- Jiang F, Chen G-L, Li J, et al. Pre gestational thalassemia screening in Mainland China: the first two years of a preventive program. Hemoglobin. 2017;41(4–6):248–253.
- Lal A, Goldrich ML, Haines DA, et al. Heterogeneity of hemoglobin H disease in childhood. N Engl J Med. 2011;364(8):710–718.