OTUD7A Regulates Neurodevelopmental Phenotypes in the 15q13.3 Microdeletion Syndrome.

Am J Hum Genet · 2018 · PMC5985537 · PMID 29395074

Europe PMC DOI

hedged sentence

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closest p · 0.0× alpha

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boldest claim

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highly significantp < 1.30 × 10 −29actually significant

The enrichment of 15q13.3 microdeletions within neurodevelopmental disorder-affected and ASD-affected case subjects (0.4% combined in NDD and ASD case subjects; 0.004% in control subjects) is highly significant (p < 1.30 × 10 −29 ).

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