Barely Significant
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An integrated transcriptomics and proteomics analysis reveals functional endocytic dysregulation caused by mutations in LRRK2.

Neurobiol Dis · 2019 · PMC6597903 · PMID 30954703

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highly significantno p-value reported
Results Our integrated -omics analysis revealed highly significant dysregulation of the endocytic pathway in iPSC-derived dopaminergic neurons carrying the LRRK2-G2019S mutation.

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