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However, in response to cell injury, the APOE-I3 mRNA is converted to the mature APOE mRNA, which is rapidly exported into the cytosol and is then translated to the corresponding protein (Xu et al

Post-hoc tests were conducted using a Bonferroni adjustment

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Beta thalassemia major is chronic hemolytic anemia and an autosomal recessive hereditary due to the complete deficiency in the synthesis of -globin chains

doi: 10.3389/fphar.2025.1585290 139 TangY.LeW