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Introduction -thalassemia is an autosomal recessive genetic disorder characterized by impaired erythropoiesis due to point mutations in the splice site or promoter sites of the -globin genes on chromosome 11

Moreover, some peaks that appeared increased in the samples exposed to the nanoformulations (Fig

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it serves as a precursor to the amino acids glutamate and glutamine, which have various roles in cellular function, including neurotransmission and nitrogen transport (Gyanwali et al., 2022)