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Parkin/PINK1-mediated mitophagy Mechanisms of Parkin/PINK1-mediated mitophagy Mutations in PINK1 (a serine/threonine kinase) 21 and Parkin (an E3 ubiquitin ligase) 22 are the most common causes of recessive forms of PD

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References to metabolic or adipose-related pathways are included for scientific context only and do not imply therapeutic or clinical outcomes

Regulation and functions of non-m(6)A mRNA modifications