Barely Significant
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Characterization of the genetic and clinical landscapes of DCTN1 gene in neurodegenerative diseases: a series of large case-control study.

NPJ Genom Med · 2025 · PMC12638979 · PMID 41271780

Europe PMCDOI
1
hedged sentence
0.0490
closest p · 1.0× alpha
0.0490
boldest claim

The sentences

nominally significantp = 0.049actually significant
A nominally significant association of DCTN1 PDVs with PD was found in the EoPD & FPD cohort (20 vs. 7, p = 0.049), which did not remain significant after correction (FDR p * = 0.098).

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