A De Novo Missense Variant in <i>TUBG2</i> in a Child with Global Developmental Delay, Microcephaly, Refractory Epilepsy and Perisylvian Polymicrogyria.

Genes (Basel) · 2022 · PMC9859306 · PMID 36672848

Europe PMC DOI

hedged sentence

0.0600

closest p · 1.2× alpha

0.0600

boldest claim

The sentences

trending towards significancep = 0.06so close (0.05 < p ≤ 0.1)

There was no difference in the mRNA level for these genes, except for GCP6 ( p = 0.01) and possibly GCP2 that was trending towards significance ( p = 0.06) ( Figure 3 B).

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