Barely Significant
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Clinical and molecular findings in actin-related inborn errors of immunity: the middle East and North Africa registry.

Front Genet · 2025 · PMC12370701 · PMID 40860338

1
hedged sentence
0.0002
closest p · 0.0× alpha
0.0002
boldest claim

The sentences

highly significantp = 0.0002actually significant
At the same time, 4 patients encountered graft-rejection, and 7 patients died of HSCT-related complications, indicating a highly significant impact of HSCT on the survival rate of patients with actinopathies ( p = 0.0002, Figure 3 ).

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