HB Tigraye OR α₂β²79(EF3)ASP→HIS(GAC→CAC): A Hemoglobin Variant with Increased Oxygen Affinity Observed in an Ethiopian Male

This publication has 10 references indexed in Scilit:

• Heterozygosity for the IVS-I-5(G→C) mutation with a G→A change at codon 18 (Val→Met; Hb Baden) in cis and a T→G mutation at codon 126 (Val→Gly; Hb Djonburi) in trans resulting in a thalassemia intermedia
  Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, 1992
• A Second Observation of the Fetal Methehoglobin Variant HB F-M-Fort Ripley or α₂^Gγ₂⁹²(F8)HIS→TYR
  Hemoglobin, 1992
• Fetal hemoglobin in normal adults and ?-thalassemia heterozygotes
  Human Genetics, 1990
• High-performance liquid chromatographic separation of human haemoglobins
  Journal of Chromatography B: Biomedical Sciences and Applications, 1988
• Separation of normal and abnormal hemoglobin chains by reversed-phase high-performance liquid chromatography
  Journal of Chromatography A, 1986
• High Performance Liquid Cbromatographic Separation of Globin Chains on a Large-Pore C₄Column
  Journal of Liquid Chromatography, 1984
• Construction of Human Gene Libraries from Small Amounts cf Peripheral Blood: Analysis of β-Like Globin Genes
  Hemoglobin, 1981
• Hemoglobin tampa:β79 (EF3) aspartic acid → tyrosine
  Biochimica et Biophysica Acta (BBA) - Protein Structure, 1980
• Oxygenation properties of hemoglobin variants with substitutions near the polyphosphate binding site
  Biochimica et Biophysica Acta (BBA) - Protein Structure, 1975
• Hemoglobin G Hsi-Tsou: β79 Asp→Gly
  Biochimica et Biophysica Acta (BBA) - Protein Structure, 1972