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Hemoglobin
international journal for hemoglobin research
Volume 31, 2007 - Issue 1
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Original

Hb Barika [α42(C7)Tyr→His (α2)] Leads to an α+-Thalassemia-like Syndrome

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Pages 17-22 | Received 07 Jul 2006, Accepted 14 Jul 2006, Published online: 07 Jul 2009

REFERENCES

  • http://globin.cse.psu.edu, Huisman THJ, Carver MFH, Efremov GD. A Syllabus of Human Hemoglobin Variants (Second Edition). Augusta: The Sickle Cell Anemia Foundation. 1998
  • http://globin.cse.psu.edu, 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 Mutat 2002; 19(3):225–233
  • Wajcman H, Galactéros F. Hemoglobins with high oxygen affinity leading to erythrocytosis. New variants and new concepts. Hemoglobin 2005; 29(2)91–106
  • Ishimori K, Morishima I, Imai K, Fushitani K, Miyazaki G, Shih D, Tame J, Pagnier J, Nigai K. NMR study of human mutant hemoglobins synthesized in Escherichia coli. Consequences of tyrosine α42 substitutions. J Biol Chem 1989; 264(25)14624–14626
  • Imai K, Fushitani K, Miyazaki G, Ishimori K, Kitagawa T, Wada Y, Morimoto H, Morishima I, Shih DT, Tame J. Site-directed mutagenesis in hemoglobin. Functional role of tyrosine-42(C7) α at the α1-β2 interface. J Mol Biol 1991; 218(4)769–778
  • Wajcman H, Préhu C, Bardakdjian-Michau J, Promé D, Riou J, Godart C, Mathis M, Hurtrel D, Galactéros F. Abnormal hemoglobins: laboratory methods. Hemoglobin 2001; 25(2)169–181
  • Wajcman H, Riou J, Yapo AP. Globin chain analysis by reversed phase high performance liquid chromatography: recent developments. Hemoglobin 2002; 26(3)271–284
  • Cartegni L, Chew SL, Krainer AR. Listening to silence and understanding nonsense: exonic mutations that affect splicing. Nat Rev Genet 2002; 3(4)285–298
  • Vasseur-Godbillon C, Marden MC, Giordano P, Wajcman H, Baudin-Creuza V. Impaired binding of AHSP to α chain variants: Hb Groene Hart illustrates a mechanism leading to unstable hemoglobins with α thalassemic like syndrome. Blood Cells Mol Dis 2006; 37(3)173–179

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