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Hereditary uveal melanoma is one of nine manifestations of the so-called TPS syndrome caused by germline mutations in the BAP1 gene (OMIM ID # 614327) (about 3% of all uveal melanomas)

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What the research shows Studies examining GHK-Cu use over periods of 2-3 months consistently show favorable safety profiles

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RAPL, a Rap1-binding molecule that mediates Rap1-induced adhesion through spatial regulation of LFA1