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A final alternative to alleviate FcRn-controlled pathological mechanisms could be to alter FcRn in itself, as may be intended with a gene therapy being developed in a collaboration between Beam and Apellis for a one-time dose of gene-editing molecules targeting FcRn [436, 437]

But they are also precisely why a thorough understanding of GHK-Cu contraindications is non-negotiable

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Singh, K., Han, K., Tilve, S., Wu, K., Geller, H