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Primary carnitine deficiency is a genetic disorder of the cellular carnitine-transporter system that typically appears by the age of five with symptoms of cardiomyopathy, skeletal-muscle weakness, and hypoglycemia

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Copper-Dependent Enzyme Activation Studies indicate that GHK-Cu provides copper for the activation of copper-dependent enzymes including lysyl oxidase (critical for collagen and elastin cross-linking), superoxide dismutase (SOD, an antioxidant enzyme), and tyrosinase