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Description
Wilson disease is a rare inherited disorder where the body cannot properly eliminate copper, leading to its accumulationmainly in the liver, brain, and eyes

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Alkaline hydrolysis of the isolated depsipeptides produced dipeptides as reported recently for cereulide and isocereulides 18

BPC-157 es inusualmente estable en el entorno gastrico debido a su derivacion de una proteina gastrica