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This process regulates mtROS accumulation via SH3GLB1, kynurenine metabolism via GOT2, and NDP52-induced mitochondrial autophagy

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Seventh, these results should not be applied to patients with primary carnitine deficiency (typically arising from genetic alterations in renal handling or muscle transport of L-carnitine) or secondary carnitine deficiency (typically arising from impaired renal tubular resorption from drug toxicity or hemodialysis)

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