MECP2 and Rett syndrome: Remarkably, most of the pathways enriched for S(+)MTZ are involved in processes typically regulated by MECP2, the gene mutated in RTT, such as chromatin organization (2 pathways), epigenetic regulation (2 pathways), and transcription (6 pathways) including, most impressively, 2 pathways regulating either MECP2‐mediated translation or the translation of MeCP2 itself (Kolberg et al. 2020; Chen et al. 2015; Della Ragione et al. 2016).