REFERENCES
- Hardison RC, Chui DHK, Giardine B, Riemer C, Patrinos GP, Anagnou N, Miller W, Wajcman H. HbVar: a relational database of human hemoglobin variants and thalassemia mutations at the globin gene server. Hum Mut 2002; 19(3)225–233,
- Patrinos GP, Giardine B, Riemer C, Miller W, Chui DHK, Anagnou NP, Wajcman H, Hardison RC. Improvements in the HbVar database of human hemoglobin variants and thalassemia mutations for population and sequence variation studies. Nucleic Acids Res 2004; 32(Database)D537–D541,
- Lacan P, Kister J, Francina A, Souillet G, Galactéros F, Delaunay J, Wajcman H. Hemoglobin Debrousse [β96(FG3)Leu→Pro]: a new unstable hemoglobin with twofold increased oxygen affinity. Am J Hematol 1996; 51(4)276–281
- Morlé F, Francina A, Ducrocq R, Wajcman H, Gonnet C, Philippe N, Souillet G, Godet J. A new α chain variant Hb Sallanches [α2 104(G11)Cys→Tyr] associated with Hb H disease in one homozygous patient. Br J Haematol 1995; 91(3)608–611
- Bayoumi RA, Dawodu A, Qureshi MM, Al-Khider A, Fitzgerald P, Riou J, Fisher CA, Fitches A, Old JM. The association of Hb Khartoum [β124(H2)Pro→Arg] with γ+-thalassemia is responsible for hemolytic disease in the newborn of a Sudanese family. Hemoglobin 1999; 23(1)33–45
- Chong SS, Boehm CD, Higgs DR, Cutting GR. Single-tube multiplex-PCR screen for common deletional determinants of α-thalassemia. Blood 2000; 95(1)360–362
- Al-Awamy BH, Niazi GA, Al-Mouzan MI, Wilson JB, Chen SS, Webber BB, Huisman THJ. Hb F-Dammam or α2Aγ2(79)(EF3)Asp→Asn. Hemoglobin 1985; 9(2)171–173
- Swiss-3DIMAGE. Swiss-Pdb Viewer. http://ca.expasy.org/cgi-bin/sw3d-search-ac, accession number: P69892
- Nakatsuji T, Lam H, Huisman THJ. Hb F-Kennestone or α2Gγ2 (EF1)77 His→Arg observed in a Caucasian baby. Hemoglobin 1983; 7(3)267–270
- Nakatsuji T, Lam H, Carver J, Huisman THJ. Hb F-Marietta or GγI80(EF4)Asp→Asn observed in a Caucasian baby. Hemoglobin 1982; 6(4)407–411
- Huisman THJ. A short review of human γ-globin gene anomalies. Acta Haematol 1987; 78(2)80–84
- Molchanova TP, Postnikov YuV, Gu L-H, Prior JF, Raven JL, Bennett JA, Huisman THJ. Hb Tigraye or α2β279(EF3)Asp→His (GAC→CAC): a hemoglobin variant with increased oxygen affinity observed in an Ethiopian male. Hemoglobin 1993; 17(3)247–250
- Pistidda P, Cherchi L, Corda M, Guiso L, Pardini S, Pirastru M, Manca L, Longinotti M, Masala B. Hb Tigraye [β79(EF3)Asp→His] in a Caucasian family from Sardinia. Hemoglobin 2001; 25(3)341–345
- Perutz MF. Molecular anatomy and physiology of hemoglobin. Disorders of Hemoglobin: Genetics, Pathophysiology and Clinical Management, MH Steinberg, BG Forget, DR Higgs, RL Nagel. Cambridge University Press, Cambridge 2001; 174–196
- Frier JA, Perutz MF. Structure of human foetal deoxyhaemoglobin. J Mol Biol 1977; 112(1)97–112
- Schneider RG, Haggard ME, Gustavson LP, Brimhall B, Jones RT. Genetic haemoglobin abnormalities in about 9000 Black and 7000 White newborns: Haemoglobin F-Dickinson (Aγ97His→Arg), a new variant. Br J Haematol 1974; 28(4)515–524
- Nakatsuji T, Lam H, Wilson JB, Webber BB, Huisman THJ. Hb F-Columbus-GA or α2Gγ294 (FG1)Asp→Asn. Hemoglobin 1982; 6(6)593–598
- De Rosa MC, Carelli Alinovi C, Schinina ME, Clementi ME, Amato A, Cappabianca MP, Pezzotti M, Giardina B. Hb Santa Clara (β97His→Asn), a human haemoglobin variant: functional characterization and structure modeling. Biochim Biophys Acta 2007; 1774(10)1299–1306