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Subsequently, changes in mitochondrial membrane potential of liver cells after METH and QR treatment were assessed using Rhodamine 123 and mitochondrial red fluorescence probes, respectively (Figures 4C, D)

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The G6PD deficiency is produced by different genetic mechanisms such as deletions, precise mutations and substitutions that affect the transcription, process or primary enzyme structure, which functionally results in a decrease of the enzymatic activity or loss of affinity by the substrate