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The Roles of ATP13A2 Gene Mutations Leading to Abnormal Aggregation of α-Synuclein in Parkinson’s Disease

6 Jul 2022

Abstract excerpt

Parkinson's disease (PD) is the second most common neurodegenerative disease. PARK9 (also known as ATP13A2) is recognized as one of the key genes that cause PD, and a mutation in this gene was first discovered in a rare case of PD in an adolescent. Lewy bodies (LBs) formed by abnormal aggregation of α-synuclein, which is encoded by the SNCA gene, are one of the pathological diagnostic criteria for PD. LBs are...

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PMID: 35875356
DOI: 10.3389/fncel.2022.927682

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 31 Aug 2026.

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