Identification of molecular signatures and pathways involved in Rett syndrome using a multi-omics approach

BACKGROUND: Rett syndrome (RTT) is a neurodevelopmental disorder mainly caused by mutations in the methyl-CpG-binding protein 2 gene (MECP2). MeCP2 is a multi-functional protein involved in many cellular processes, but the mechanisms by which its dysfunction causes disease are not fully understood....

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Detalles Bibliográficos
Autores principales: Pascual-Alonso, Ainhoa, Xiol, Clara, Smirnov, Dmitrii, Kopajtich, Robert, Prokisch, Holger, Armstrong, Judith
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10503149/
https://www.ncbi.nlm.nih.gov/pubmed/37710353
http://dx.doi.org/10.1186/s40246-023-00532-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10503149/
https://www.ncbi.nlm.nih.gov/pubmed/37710353
http://dx.doi.org/10.1186/s40246-023-00532-1

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