Barely Significant
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Multiplex gene and phenotype network to characterize shared genetic pathways of epilepsy and autism.

Sci Rep · 2021 · PMC7806931 · PMID 33441621

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highly significantno p-value reported
In summary, the relatively large number of BEGs and their highly significant enrichment further support the functional relevance of these two modules in the shared etiology between epilepsy and autism, and possibly other developmental disorders.

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