Barely Significant
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De novo mutations in PLXND1 and REV3L cause Möbius syndrome.

Nat Commun · 2015 · PMC4648025 · PMID 26068067

Europe PMCDOI
1
hedged sentence
0.0047
closest p · 0.1× alpha
0.0047
boldest claim

The sentences

highly significantP value=0.0047actually significant
Analysis of the subarachnoid space at E16.5 in Rev3l +/ − mice revealed a highly significant increase in subarachnoid volume ( t -test, P value=0.0047; Fig. 3a ).

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