Barely Significant
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Use of whole genome sequencing to determine the genetic basis of visceral myopathies including Prune Belly syndrome.

J Rare Dis (Berlin) · 2023 · PMC10241726 · PMID 37288276

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hedged sentence
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closest p · 0.0× alpha
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boldest claim

The sentences

highly significantp = 1.1 × 10 −7actually significant
There was only one highly significant gene identified ( ACTG2 ( p = 1.1 × 10 −7 )) from the assembled alleles (Fig. 1 D and Supplementary Table S 5 ).

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