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Nanomedical approaches to deplete intracellular glutathione in oncology - ScienceDirect
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FRDA is caused by the expansion of guanine–adenine–adenine (GAA) trinucleotide repeats in the first intron of the frataxin ( FXN ) gene on chromosome 9q21.11, leading to substantially decreased levels of mitochondrial protein FXN [5]
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