Global Impairment of Immediate-Early Genes Expression in Rett Syndrome Models and Patients Linked to Myelination Defects

Rett syndrome (RTT) is a severe neurodevelopmental disease caused almost exclusively by mutations to the MeCP2 gene. This disease may be regarded as a synaptopathy, with impairments affecting synaptic plasticity, inhibitory and excitatory transmission and network excitability. The complete understan...

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Detalles Bibliográficos
Autores principales: Petazzi, Paolo, Jorge-Torres, Olga Caridad, Gomez, Antonio, Scognamiglio, Iolanda, Serra-Musach, Jordi, Merkel, Angelika, Grases, Daniela, Xiol, Clara, O’Callaghan, Mar, Armstrong, Judith, Esteller, Manel, Guil, Sonia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9864472/
https://www.ncbi.nlm.nih.gov/pubmed/36674969
http://dx.doi.org/10.3390/ijms24021453

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9864472/
https://www.ncbi.nlm.nih.gov/pubmed/36674969
http://dx.doi.org/10.3390/ijms24021453

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