Linkage and exome analysis implicate multiple genes in non-syndromic intellectual disability in a large Swedish family.

BMC Med Genomics · 2019 · PMC6833288 · PMID 31694657

Europe PMC DOI

hedged sentence

0.0580

closest p · 1.2× alpha

0.0580

boldest claim

The sentences

did not reach statistical significancep = 0.058so close (0.05 < p ≤ 0.1)

The TPR gene showed significant association with affected status in the family, while ACOT4 did not reach statistical significance ( p = 0.058).

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