Monoallelic Mutations in <i>CC2D1A</i> Suggest a Novel Role in Human Heterotaxy and Ciliary Dysfunction.

Circ Genom Precis Med · 2020 · PMC7748040 · PMID 33196317

Europe PMC DOI

hedged sentence

0.2818

closest p · 5.6× alpha

0.2818

boldest claim

The sentences

did not reach statistical significanceP =0.2818not close (p > 0.1)

Mirrored digestive system was also observed but did not reach statistical significance ( P =0.2818, Figure 5 B).

also in 111,027 other papers

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.