Barely Significant
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Long-read sequencing enables comprehensive molecular genetic diagnosis of Fabry disease.

Hum Genomics · 2024 · PMC11603755 · PMID 39609713

Europe PMCDOI
1
hedged sentence
0.0001
closest p · 0.0× alpha
0.0001
boldest claim

The sentences

extremely significantp < 0.0001actually significant
Enzyme activity in the male group was significantly lower than in the female group, with an extremely significant decrease ( p < 0.0001).

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