Barely Significant
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DNMT3A Haploinsufficiency Results in Behavioral Deficits and Global Epigenomic Dysregulation Shared across Neurodevelopmental Disorders.

Cell Rep · 2020 · PMC7716597 · PMID 33238114

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highly significantno p-value reported
GAGE analysis revealed highly significant, concordant changes in gene expression in DNMT3A KO/+ for gene sets dysregulated in DNMT3A Baf53b- cKO and MeCP2 mutants ( Figure 6F ).

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