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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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Detalles Bibliográficos
Autores principales:	Bou-Fakhredin, Rayan, De Franceschi, Lucia, Motta, Irene, Eid, Assaad A., Taher, Ali T., Cappellini, Maria Domenica
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2022
Materias:	Review
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9138068/ https://www.ncbi.nlm.nih.gov/pubmed/35624830 http://dx.doi.org/10.3390/antiox11050967

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