Barely Significant
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Neurological manifestations and genotype-phenotype correlations in <i>NDUFAF6</i>-associated mitochondrial disease.

Brain Commun · 2026 · PMC13036829 · PMID 41924699

Europe PMCDOI
1
hedged sentence
0.0005
closest p · 0.0× alpha
0.0005
boldest claim

The sentences

highly significantP < 0.0005actually significant
A P -value < 0.05 (*) was considered statistically significant, P < 0.005 (**) was considered highly significant, and P < 0.0005 (***) was considered extremely significant.

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