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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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TJs are assembled by a group of interacting proteins including zonula occludens (ZO)-1, claudins, and occludins [4]
BPC-157 es inusualmente estable en el entorno gastrico debido a su derivacion de una proteina gastrica
Transporter Reversal as a Survival Exit Valve
PMID: 35000410
