MECP2 mutations affect ciliogenesis: a novel perspective for Rett syndrome and related disorders

Mutations in MECP2 cause several neurological disorders of which Rett syndrome (RTT) represents the best‐defined condition. Although mainly working as a transcriptional repressor, MeCP2 is a multifunctional protein revealing several activities, the involvement of which in RTT remains obscure. Beside...

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Detalles Bibliográficos
Autores principales: Frasca, Angelisa, Spiombi, Eleonora, Palmieri, Michela, Albizzati, Elena, Valente, Maria Maddalena, Bergo, Anna, Leva, Barbara, Kilstrup‐Nielsen, Charlotte, Bianchi, Federico, Di Carlo, Valerio, Di Cunto, Ferdinando, Landsberger, Nicoletta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7278541/
https://www.ncbi.nlm.nih.gov/pubmed/32383329
http://dx.doi.org/10.15252/emmm.201910270

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7278541/
https://www.ncbi.nlm.nih.gov/pubmed/32383329
http://dx.doi.org/10.15252/emmm.201910270

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