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A commonly reported figure is one in 30,000 people in the world, according to studies conducted before researchers discovered its genetic causeany one of a number of possible mutations in the bodys ATP7B gene, which is involved in transporting copper in the body

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This already complex picture is further complicated by the recent discovery of branched ubiquitin chains, which contain non-homogeneous lysine linkages

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Moreover, MET is highly expressed in cortical areas involved in attention, memory, and sensorimotor functions 24