Multimodal Neuroimaging in Rett Syndrome With MECP2 Mutation
Sign Up to like & getrecommendations! Published in 2022 at "Frontiers in Neurology"
DOI: 10.3389/fneur.2022.838206
Abstract: Rett syndrome (RTT) is a rare neurodevelopmental disorder characterized by severe cognitive, social, and physical impairments resulting from de novo mutations in the X-chromosomal methyl-CpG binding protein gene 2 (MECP2). While there is still no… read more here.
Keywords: neuroimaging rett; rett syndrome; syndrome mecp2; mecp2 mutation ... See more keywords