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. 2021 Apr 1;9:636506. doi: 10.3389/fcell.2021.636506

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Copyright © 2021 Nicoletti, Palermo, Del Prete, Mancuso and Ceravolo.

This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

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Mechanisms and genes involved in mitochondrial dysfunction in Parkinson’s disease. ATP13A2, ATPase cation transporting 13A2; DJ-1, protein deglycase; LRRK2, leucine-rich repeat kinase 2; PINK1, phosphatase and tensin homolog (PTEN)-induced putative kinase 1; VPS35, vacuolar protein sorting 35.