Enrichment of mutations in chromatin regulators in people with Rett syndrome lacking mutations in MECP2.

Using the DAVID functional annotation tool ( https://david.ncifcrf.gov/ ) we found that there was a highly significant enrichment of the term “chromatin regulator” (uncorrected p = 0.00011; Benjamini-Hochberg corrected p = 0.0068) of the Protein Information Resource (PIR) database.

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