Targeted transcript analysis in muscles from patients with genetically diverse congenital myopathies.

Brain Commun · 2022 · PMC9525005 · PMID 36196089

Europe PMC DOI

hedged sentence

0.0600

closest p · 1.2× alpha

0.0600

boldest claim

The sentences

did not achieve significanceP = 0.06so close (0.05 < p ≤ 0.1)

4E ) though in AR RYR1 MmD/CNM MBNL1 levels were reduced though the fold change did not achieve significance (the mean log 2 -fold change was −0.57 adjusted P = 0.06; Fig. 4F ).

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