Barely Significant
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Inherited Retinal Degeneration Caused by Dehydrodolichyl Diphosphate Synthase Mutation-Effect of an <i>ALG6</i> Modifier Variant.

Int J Mol Sci · 2024 · PMC10816542 · PMID 38256083

1
hedged sentence
0.3900
closest p · 7.8× alpha
0.3900
boldest claim

The sentences

did not reach statistical significancep = 0.39not close (p > 0.1)
Progressive thinning of the foveal ONL showed a tendency for greater severity in patients with the ALG6 variant ( Figure 3 C), but this did not reach statistical significance ( p = 0.39).

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