Royal Society of Chemistry, MedChemComm, 11(10), p. 1900-1906, 2019
DOI: 10.1039/c9md00291j
Full text: Unavailable
The intracellular polymerization and the concomitant sickling processes, central to the pathology of sickle cell disease, can be mitigated by increasing the oxygen affinity of sickle hemoglobin (HbS).