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Proteome Wide Association Studies of LRRK2 variants identify novel causal and druggable for Parkinson’s disease

2023-01-07

Abstract excerpt

Common and rare variants in the LRRK2 locus are associated with Parkinson’s disease (PD) risk, but the downstream effects of these variants on protein levels remains unknown. We performed comprehensive proteogenomic analyses using the largest aptamer-based CSF proteomics study to date (7,006 aptamers (6,138 unique proteins) in 3,107 individuals). We identified eleven independent SNPs in the LRRK2 locus associated...

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Literature Corpus work
d5480d62-f3cd-5707-81b3-9c4ee62bf49f
DOI
10.1101/2023.01.05.23284241
Open publication

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Proteome Wide Association Studies of LRRK2 variants identify novel causal and druggable for Parkinson’s diseaseDOI 10.1101/2023.01.05.23284241
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