<i>PCDH19</i>-related epilepsy in mosaic males: The phenotypic implication of genotype and variant allele frequency.

Front Neurol · 2022 · PMC9669318 · PMID 36408521

Europe PMC DOI

hedged sentence

0.1820

closest p · 3.6× alpha

0.1820

boldest claim

The sentences

did not reach statistical significancep = 0.182not close (p > 0.1)

Patients with high VAF also had a median DD/ID severity that was 1.5 units greater than patients with low VAF, though results did not reach statistical significance ( p = 0.182).

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