The Roles of ATP13A2 Gene Mutations Leading to Abnormal Aggregation of α-Synuclein in Parkinson’s Disease
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DOI: 10.3389/fncel.2022.927682
Abstract: 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… read more here.
Keywords: atp13a2 gene; abnormal aggregation; disease; aggregation synuclein ... See more keywords