Barely Significant
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A Restricted Repertoire of De Novo Mutations in ITPR1 Cause Gillespie Syndrome with Evidence for Dominant-Negative Effect.

Am J Hum Genet · 2016 · PMC4863663 · PMID 27108798

1
hedged sentence
0.0015
closest p · 0.0× alpha
0.0015
boldest claim

The sentences

highly significantp ≤ 0.0015actually significant
We observe a highly significant difference (p ≤ 0.0015) with the dominant-negative mutations inducing a lesser change in protein stability than the two other groups of mutations.

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Quoted from the open-access full text in Europe PMC under the licence the publisher applied. The sentence is reproduced exactly as published; the emphasis is ours.