Abnormal Expression of Cerebrospinal Fluid Cation Chloride Cotransporters in Patients with Rett Syndrome

OBJECTIVE: Rett Syndrome is a progressive neurodevelopmental disorder caused mainly by mutations in the gene encoding methyl-CpG-binding protein 2. The relevance of MeCP2 for GABAergic function was previously documented in animal models. In these models, animals show deficits in brain-derived neurot...

Descripción completa

Detalles Bibliográficos
Autores principales: Duarte, Sofia Temudo, Armstrong, Judith, Roche, Ana, Ortez, Carlos, Pérez, Ana, O’Callaghan, Maria del Mar, Pereira, Antonina, Sanmartí, Francesc, Ormazábal, Aida, Artuch, Rafael, Pineda, Mercedes, García-Cazorla, Angels
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3716803/
https://www.ncbi.nlm.nih.gov/pubmed/23894354
http://dx.doi.org/10.1371/journal.pone.0068851

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3716803/
https://www.ncbi.nlm.nih.gov/pubmed/23894354
http://dx.doi.org/10.1371/journal.pone.0068851

Ejemplares similares