Barely Significant
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Expanding the clinical-pathological and genetic spectrum of RYR1-related congenital myopathies with cores and minicores: an Italian population study.

Acta Neuropathol Commun · 2022 · PMC9013059 · PMID 35428369

Europe PMCDOI
1
hedged sentence
0.0390
closest p · 0.8× alpha
0.0390
boldest claim

The sentences

nominally significantp = 0.039actually significant
The association between mutations in NTD-A with facial weakness and delayed independent ambulation was nominally significant (Fisher exact test p = 0.039, p = 0.038, respectively).

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