Barely Significant
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A novel spliceosomopathy caused by de novo SF3B3 variants.

Genome Med · 2026 · PMC13023183 · PMID 41709284

Europe PMCDOI
1
hedged sentence
0.0100
closest p · 0.2× alpha
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boldest claim

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highly significantp < 0.01actually significant
In contrast, fibroblasts from patient 8 exhibited a highly significant increase in the G2/M population (20.5% vs. ~14–16% in controls; p < 0.01), suggesting impaired progression through the G2/M checkpoint (Additional file 2: Fig S21).

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