Article
Compromised immune/inflammatory responses in Rett syndrome.
Free radical biology & medicine - 20 May 2020
Pecorelli Alessandra, Cervellati Carlo, Cordone Valeria, Hayek Joussef, Valacchi Giuseppe
Abstract excerpt
Mutations in X-linked gene methyl-CpG-binding protein 2 (MECP2), a key transcriptional regulator, account for most cases of Rett syndrome (RTT), a devastating neurodevelopmental disorder with no known cure. Despite extensive research to elucidate MeCP2 functions, the mechanisms underlying RTT pathophysiology are still unclear. In addition to a variety of neurological symptoms, RTT also includes a plethora of...
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