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Redox Balance in β-Thalassemia and Sickle Cell Disease: A Love and Hate Relationship

β-thalassemia and sickle cell disease (SCD) are inherited hemoglobinopathies that result in both quantitative and qualitative variations in the β-globin chain. These in turn lead to instability in the generated hemoglobin (Hb) or to a globin chain imbalance that affects the oxidative environment bot...

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Bibliographic Details
Main Authors:	Rayan Bou-Fakhredin (Author), Lucia De Franceschi (Author), Irene Motta (Author), Assaad A. Eid (Author), Ali T. Taher (Author), Maria Domenica Cappellini (Author)
Format:	Book
Published:	MDPI AG, 2022-05-01T00:00:00Z.
Subjects:	article
Online Access:	Connect to this object online.
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