ghk-cu wilson's disease – Treating a Rare But Curable Movement Disorder Wilson disease liver copper accumulation
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European journal of endocrinology / European Federation of Endocrine Societies

40, 2023, p

Its more increased by depth, so thats something you could play around with as well
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Larsson A, Mattsson B, Wauters EA, van Gool JD, Duran M, Wadman SK: 5-oxoprolinuria due to hereditary 5-oxoprolinase deficiency in two brothers--a new inborn error of the gamma-glutamyl cycle