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Mitochondrial and Clearance Impairment in p.D620N VPS35 Patient‐Derived Neurons

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VPS35 is part of the retromer complex and is responsible for the trafficking and recycling of proteins implicated in autophagy and lysosomal degradation, but also takes part in the degradation… Click to show full abstract

VPS35 is part of the retromer complex and is responsible for the trafficking and recycling of proteins implicated in autophagy and lysosomal degradation, but also takes part in the degradation of mitochondrial proteins via mitochondria‐derived vesicles. The p.D620N mutation of VPS35 causes an autosomal‐dominant form of Parkinson's disease (PD), clinically representing typical PD.

Keywords: impairment d620n; mitochondrial clearance; vps35 patient; clearance impairment; d620n vps35; patient derived

Journal Title: Movement Disorders
Year Published: 2020

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