Hb Setif or α294(G1)Asp→Tyrβ2 Observed in a Saudi Arabian Family

This publication has 12 references indexed in Scilit:

• Hemoglobin setif and in vitro pseudosickling noted in a family with co-existent α and β thalassemia
  Pathology, 1983
• Separation of tryptic peptides of normal and abnormal a, β, γ, and δ hemoglobin chains by high-performance liquid chromatography
  Journal of Chromatography A, 1979
• Micro‐sequence analysis of peptides and proteins using 4‐NN‐dimethylaminoazobenzene 4′‐isothiocyanate/phenylisothiocyanate double coupling method
  FEBS Letters, 1978
• Hemoglobin Setif (α94 (G1) ASP → TYR) in Iran a Report of 9 Cases
  Hemoglobin, 1977
• Separation of Human Hemoglobins by Deae-Cellulose Chromatography using Glycine-Kcn-Nacl Developers
  Hemoglobin, 1976
• Hemoglobin Riyadh-α₂β₂(120 [GH3] Lys→Asn): A New Variant Found in Association with α-Thalassemia and Iron Deficiency
  Hemoglobin, 1976
• Hb Setif: G1 (94)α Asp → Tyr a new α chain hemoglobin variant with substitution of the residue involved in a hydrogen bond between unlike subunits
  FEBS Letters, 1972
• Three-dimensional Fourier Synthesis of Horse Oxyhaemoglobin at 2.8 Å Resolution: The Atomic Model
  Nature, 1968
• Abnormal human haemoglobins: Separation and characterization of the α and β chains by chromatography, and the determination of two new variants, Hb chesapeake and Hb J (Bangkok)
  Journal of Molecular Biology, 1966
• PROTEIN COAGULATION AND ITS REVERSAL
  The Journal of general physiology, 1930