To the Editor Sickle cell disease (SCD) is an inherited hemoglobinopathy caused by a single amino acid substitution at the sixth residue of the beta (β)-globin subunit (p.Glu6Val) Vaso-occlusion, hemolytic anemia and vasculopathy are the hallmarks of SCD pathophysiology, leading to high morbility and mortality.
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Torti et al. (2026) studied this question.
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