Hb Arta [β45 (CD4) Phe→Cys]: a new unstable haemoglobin with reduced oxygen affinity in trans with β‐thalassaemiaGeorge Vassilopoulos, Dimitris Loukopoulos, Claire Poyart et al.|British Journal of Haematology|1995Cited by 15
Modulating the oxygen affinity of human fetal haemoglobin with synthetic allosteric modulatorsIoannis Papassotiriou, Claire Poyart, J. Kister et al.|British Journal of Haematology|1998Cited by 13
Hb Montfermeil [β 130(H8) Tyr→Cys]: suggests a key role for the interaction between helix A and H in oxygen affinity of the hemoglobin moleculeJ. Kister, Henri Wajcman, Véronique Baudin‐Creuza et al.|Blood Cells Molecules and Diseases|2005Cited by 13
The homozygous state for Hb Crete [β129 (H7) Ala→Pro] is associated with a complex phenotype including erythrocytosis and functional anemiaIoannis Papassotiriou, Emmanuel Kanavakis, Alexandra Stamoulakatou et al.|Blood Cells Molecules and Diseases|2005Cited by 13