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In 1993, it was discovered that Wilsons disease was caused by a mutation in the ATP7B gene, on chromosome 13, which resulted in absent or reduced function of a copperchaperone protein, ATP7B.14 ATP7B is a metal-transporting P-type ATPase, located on the trans-Golgi complex of the hepatocyte.15 The ATP7B protein is necessary for transport of copper into vesicles that form lysosomes for excretion into the bile

Our unique blend includes glutathione, known as the ultimate skin-brightening agent, which works to inhibit melanin production, providing you with a clearer and more uniform complexion

pilot study) and standard oral Setria glutathione at 500-1,000 mg/day (slower but demonstrated over six months in the Richie et al