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Abstract Wilson's disease (WD) is an inborn error of copper metabolism caused by a mutation to the copper-transporting gene ATP7B
Product Specifications Compound Type: Copper-binding tripeptide complex Classification: Regenerative signaling peptide Primary Structure: Glycyl-L-histidyl-L-lysine copper complex Molecular Formula: CHNOCu Molecular Weight: ~403.93 g/mol Administration Route: Subcutaneous or topical application observed in research settings Stability Profile: High stability copper-peptide complex Development Status: Advanced research phase Research Focus: Skin remodeling pathways, collagen support signaling, follicular research, antioxidant activity, and tissue recovery models Quality Commitment SlimFit Compounds partners with emerging U.S.-based manufacturers that adhere to strict production, verification, and purity standards
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Vitamin B12 works with folate in methylation, so B12 deficiency worsens homocysteine problems from MTHFR
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