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Article title
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Abstract
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Keywords
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Introduction
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Need for change in treatment strategies for β-thalassemia
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Erythropoiesis stimulation agents
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Increasing fetal hemoglobin expression
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Innovative approaches to enhancing traditional therapies for reducing iron overload
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Hepcidin synthesis modifiers
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Development of new chelating molecules
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Gene therapy for beta-thalassemia
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Gene supplementation via lentiviral vectors
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Precision editing techniques
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Allogeneic hematopoietic stem cell transplantation in TDT
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Conclusion
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Ethical statement
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Conflict of interest
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Use of AI
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Funding
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Author contributions
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Acknowledgements
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Reference
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