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Wilson's disease (excess build-up of copper) Wilson's disease is a very rare genetic condition as both parents must carry the defective ATP7B gene to pass it on
Subsequent research using intermittent protocols achieved comparable neuroplastic outcomes with less total compound exposure and presumably lower risk of tolerance development
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Outcome ascertainment The primary outcome for this study was a modified version of the 3-point MACE (3P-MACE), defined as occurrence of myocardial infarction, stroke, or all-cause death
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