Multimodal Neuroimaging in Rett Syndrome With MECP2 Mutation

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 cure for RTT, exploring up-to date neurofunctional di...

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Detalles Bibliográficos
Autores principales: Kong, Yu, Li, Qiu-bo, Yuan, Zhao-hong, Jiang, Xiu-fang, Zhang, Gu-qing, Cheng, Nan, Dang, Na
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Neurology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8904872/
https://www.ncbi.nlm.nih.gov/pubmed/35280272
http://dx.doi.org/10.3389/fneur.2022.838206

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8904872/
https://www.ncbi.nlm.nih.gov/pubmed/35280272
http://dx.doi.org/10.3389/fneur.2022.838206

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