Genome-wide screening for genes involved in the epigenetic basis of fragile X syndrome.

Stem Cell Reports · 2022 · PMC9133649 · PMID 35427485

Europe PMC DOI

hedged sentence

0.0900

closest p · 1.8× alpha

0.0900

boldest claim

The sentences

did not reach statistical significancep = 0.09so close (0.05 < p ≤ 0.1)

DNA-methylation analysis of the FMR1 promoter in the mutated samples identified an overall decrease in DNA methylation in the C6orf57 mutant, but it did not reach statistical significance (p = 0.09; Figure S3 C).

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