Unraveling Molecular Pathways Altered in MeCP2-Related Syndromes, in the Search for New Potential Avenues for Therapy

Methyl-CpG-binding protein 2 (MeCP2) is an X-linked epigenetic modulator whose dosage is critical for neural development and function. Loss-of-function mutations in MECP2 cause Rett Syndrome (RTT, OMIM #312750) while duplications in the Xq28 locus containing MECP2 and Interleukin-1 receptor-associat...

Descripción completa

Detalles Bibliográficos
Autores principales: Castells, Alba-Aina, Balada, Rafel, Tristán-Noguero, Alba, O’Callaghan, Mar, Cortès-Saladelafont, Elisenda, Pascual-Alonso, Ainhoa, Garcia-Cazorla, Àngels, Armstrong, Judith, Alcántara, Soledad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7913493/
https://www.ncbi.nlm.nih.gov/pubmed/33546327
http://dx.doi.org/10.3390/biomedicines9020148

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7913493/
https://www.ncbi.nlm.nih.gov/pubmed/33546327
http://dx.doi.org/10.3390/biomedicines9020148

Ejemplares similares