NRXN1 and epilepsy: These microdeletions affected 158 protein-coding RefSeq genes and exhibited an enrichment of genes previously associated with epilepsy (NRXN1, RBFOX1, PCDH7, KCNA2, EPM2A, RORB, PLCB1) and neuropsychiatric disorders (DPYD, CADM2, PARK2, GRM8, TSNARE1, TPH2, MACROD2) (Table 3).