WGCNA Identifies Translational and Proteasome-Ubiquitin Dysfunction in Rett Syndrome

Rett Syndrome (RTT) is an X linked neurodevelopmental disorder caused by mutations in the methyl-CpG-binding protein 2 (MECP2) gene, resulting in severe cognitive and physical disabilities. Despite an apparent normal prenatal and postnatal development period, symptoms usually present around 6 to 18...

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Detalles Bibliográficos
Autores principales: Haase, Florencia, Gloss, Brian S., Tam, Patrick P. L., Gold, Wendy A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8465861/
https://www.ncbi.nlm.nih.gov/pubmed/34576118
http://dx.doi.org/10.3390/ijms22189954

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8465861/
https://www.ncbi.nlm.nih.gov/pubmed/34576118
http://dx.doi.org/10.3390/ijms22189954

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