Reduced Gamma Oscillations in a Mouse Model of Intellectual Disability: A Role for Impaired Repetitive Neurotransmission?

Intellectual disability affects 2–3% of the population; mutations of the X-chromosome are a major cause of moderate to severe cases. The link between the molecular consequences of the mutation and impaired cognitive function remains unclear. Loss of function mutations of oligophrenin-1 (OPHN1) disru...

Descripción completa

Detalles Bibliográficos
Autores principales: Powell, Andrew D., Saintot, Pierre-Philippe, Gill, Kalbinder K., Bharathan, Ashtami, Buck, S. Caroline, Morris, Gareth, Jiruska, Premysl, Jefferys, John G. R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4011727/
https://www.ncbi.nlm.nih.gov/pubmed/24800744
http://dx.doi.org/10.1371/journal.pone.0095871

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4011727/
https://www.ncbi.nlm.nih.gov/pubmed/24800744
http://dx.doi.org/10.1371/journal.pone.0095871

Ejemplares similares