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Thalassemia can be defined as a genetic disorder which, under the circumstances of α- or β-globin chain anomalies, presents with impaired or completely deficient synthesis of the hemoglobin (69, 70)
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doi: 10.3389/fcell.2020.603837 Received 08 September 2020 Accepted 30 November 2020 Published 12 January 2021 Volume 8 - 2020 Edited by Sergio Giannattasio, Consiglio Nazionale delle Ricerche, Istituto di Biomembrane, Bioenergetica e Biotecnologie Molecolari (IBIOM), Italy Reviewed by Cesare Indiveri, University of Calabria, Italy
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