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doi: 10.1016/j.plaphy.2023.108229 57 KadotaY.FuruichiT.SanoT.KayaH.GunjiW.MurakamiY.et al

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From the genetics angle, there are some pediatric, congenital causes of 5-oxoprolinuria which not surprisingly involved defects in enzymes of the gamma-glutamyl cycle (in particular, mutations in glutathione synthetase and 5-oxoprolinase have been identified in these patients).

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Angelova PR, Abramov AY (2018) Role of mitochondrial ROS in the brain: from physiology to neurodegeneration

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Oxid Med Cell Longev 5:114

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Howard A

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