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440 ATP7B encodes a transmembrane copper transport ATPase, and mutations in ATP7B cause Wilsons disease by impairing copper homeostasis, leading to copper overload in the liver, brain, and other organs
In some cases, BPC-157 may also be available in oral or topical forms, though injections are often preferred for their direct and potent effects
doi:10.1183/09031936.04.00016804 6 Rushworth, G
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