Abstract Rett syndrome (RTT) is a progressive neurodevelopmental disorder. mainly caused by mutations in MeCP2 and currently with no cure. We report here that neurons from R106W MeCP2 RTT human iPSCs as well as human embryonic stem cells after MeCP2 knockdown exhibit consistent and long-lasting impairment in maturation as indicated by impaired action potentials and passive membrane pr... https://beqmgbo7t1lkw.bloginwi.com/68598711/ideologies-and-discourses-extreme-narratives-in-extreme-metal-music