State‐of‐the‐art therapies for Rett syndrome

Rett syndrome (RTT) is an X‐linked neurogenetic disorder caused by mutations of the MECP2 (methyl‐CpG‐binding protein 2) gene. Over two decades of work established MeCP2 as a protein with pivotal roles in the regulation of the epigenome, neuronal physiology, synaptic maintenance, and behaviour. Give...

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Detalles Bibliográficos
Autores principales: Panayotis, Nicolas, Ehinger, Yann, Felix, Marie Solenne, Roux, Jean‐Christophe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Reviews
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10087176/
https://www.ncbi.nlm.nih.gov/pubmed/36056801
http://dx.doi.org/10.1111/dmcn.15383

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10087176/
https://www.ncbi.nlm.nih.gov/pubmed/36056801
http://dx.doi.org/10.1111/dmcn.15383

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