Barely Significant
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Rare genetic variation in mitochondrial pathways influences the risk for Parkinson's disease.

Mov Disord · 2018 · PMC6282592 · PMID 30256453

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nominally significantno p-value reported
Moreover, none of the top 10 nominally significant genes replicated across both the ParkWest and PPMI cohorts (Table 1 ).

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