References
- Hardison RC, Chui DHK, Giardine B, et al. HbVar: A relational database of human hemoglobin variants and thalassemia mutations at the globin gene server. Hum Mutat. 2002;19(3):225–233
- Kountouris P, Lederer CW, Fanis P, et al. IthaGenes: An interactive database for haemoglobin variations and epidemiology. PLoS One. 2014;9(7):e103020. doi: 10.1371/journal.pone.0103020
- Zanella-Cleon I, Becchi M, Lacan P, et al. Detection of a thalassemic α-chain variant (Hemoglobin Groene Hart) by reversed-phase liquid chromatography. Clin Chem. 2008;54(6):1053–1059
- Honig GR, Shamsuddin M, Zaizov R, et al. Hemoglobin Petah Tikva (α110 Ala → Asp): A new unstable variant with α-thalassemia-like expression. Blood. 1981;57(4):705–711
- Ohba Y, Fujisawa K, Imai K, et al. A new α chain variant Hb Tonosho [α 110(G17)Ala → Thr]: Subunit dissociation during cation exchange chromatography for Hb A1c assay. Hemoglobin. 1990;14(4):413–422
- Wajcman H, Vasseur C, Blouquit Y, et al. Unstable α-chain hemoglobin variants with factitious β-thalassemia biosynthetic ratio: Hb Questembert (α131[H14]Ser → Pro) and Hb Caen (α132[H15]Val → Gly). Am J Hematol. 1993;42(4):367–374
- Lacan P, Drai J, Aubry M, et al. A new β-globin variant: Hb Sainte Eugénie [β104(G6)Arg → Trp] in a French Caucasian female. Hemoglobin. 2000;24(3):245–248
- Promé D, Promé JC, Déon C, et al. Structural determination of a new electrophoreticaly silent variant: Hemoglobin Alzette, β104(G6)Arg → Lys. Rapid Commun Mass Spectrom. 1995;Spec No:S165–168
- Ryrie DR, Plowman D, Lehmann H. Haemoglobin Sherwood Forest β104(G6)Arg → Thr. FEBS Lett. 1977;83(2):260–262
- Baiget M, Gomez Pereira C, Jue DL, et al. A case of Hemoglobin Indianapolis [β112(G14)Cys → Arg] in an individual from Cordoba, Spain. Hemoglobin. 1986;10(5):483–494
- Brennan SO, Potter HC, Kubala LM, et al. Hb Canterbury [β112(G14)Cys → Phe]: A new, mildly unstable variant. Hemoglobin. 2002;26(1):67–69
- Harano T, Harano K, Kushida Y, et al. A new abnormal variant, Hb Yahata or β112(G14)Cys → Tyr, found in a Japanese: Structural confirmation by DNA sequencing of the β-globin gene. Hemoglobin. 1991;15(1–2):109–113
- Harano T, Harano K, Kawasaki R, Kawakami K. Hb Toranomon [β112(G14)Cys → Trp]: A new unstable electrophoretically silent hemoglobin. Hemoglobin. 1996;20(4):361–369
- Finlayson J, Ghassemifar R, Holmes P, et al. Hb East Timor [β80(EF4)Asn → His, AAC > CAC (HBB c.241A > C)], a variant hemoglobin associated with normal hematology. Hemoglobin. 2010;34(6):561–564
- Blackwell RQ, Yang HJ, Wang CC. Hemoglobin G Szuhu: β80 Asn → Lys. Biochim Biophys Acta. 1969;188(1):59–64
- Schmidt RM, Bechtel KC, Johnson MH, et al. Hemoglobin Lufkin: β29(B11)Gly → Asp. An unstable hemoglobin variant involving an internal amino acid residue. Hemoglobin. 1977;1(8):799–814
- Lacan P, Becchi M, Zanella-Cleon I, et al. Two new β chain variants: Hb Tripoli [β26(B8)Glu → Ala] and Hb Tizi-Ouzou [β29(B11)Gly → Ser]. Hemoglobin. 2004;28(3):205–212