Article

Comprehensive assessment of <i>PINK1</i> variants in Parkinson’s disease

2020-01-27

Abstract excerpt

Multiple genes have been associated with monogenic Parkinson’s disease and Parkinsonism syndromes. Mutations in PINK1 (PARK6) have been shown to result in autosomal recessive early onset Parkinson’s disease. In the past decade, several studies have suggested that carrying a single heterozygous PINK1 mutation is associated with increased risk for Parkinson’s disease. Here we comprehensively assess the role of PINK1...

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Literature Corpus work: 8bbe3dba-27de-53f7-8238-31511f98d026
DOI: 10.1101/2020.01.21.20018101

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