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Genetic defects in alanine-glyoxylate transaminase (either low activity or, rarely, a mutation that leads to the enzyme being in mitochondria rather than peroxisomes) results in hyperoxaluria
CS has been shown to induce a number of different antioxidant defenses including the expression of enzymes and transcription factors that lead to increased synthesis of GSH [14]
MV: Data curation, Formal analysis, Investigation, Software, Visualization, Writing original draft
Frequently Asked Questions What is the CAS number for GHK-Cu
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