Barely Significant
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Molecular and phenotypic abnormalities in individuals with germline heterozygous PTEN mutations and autism.

Mol Psychiatry · 2015 · PMC4388743 · PMID 25288137

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The sentences

highly significantp -value = 2.76×10 −8actually significant
Comparing the full set of 1377 differentially expressed genes to those contained within the gene ontology term “central nervous system myelination” (accession number GO:0022010), we found highly significant enrichment of myelination-related genes (Fisher’s exact test, odds ratio = 3.66, p -value = 2.76×10 −8 ).

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