IndraLab

Statements



"UCH-L1 mutations are linked to autosomal-dominant PD, however the mechanism by which it caused the disease is unclear, with conflicting evidence reported for its in vivo functions. Recent studies reveal a role for UCH-L1 in chaperone-mediated autophagy (CMA) and mutant UCH-L1 was shown to inhibit CMA-mediated removal of alpha-synuclein [83]."