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Mutations in SNCA , LRRK2 and VPS35 genes were associated with autosomal dominant PD, while mutations in PINK1 , PARK7/DJ-1 , PARK2/PARKIN , PLA2G6 , ATP13A2 , and FBXO7 cause autosomal recessive PD and/or parkinsonism [74]

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Further studies are necessary to fully characterize its biological mechanisms and broader applications within biomedical science

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