Auditory sensory memory span for duration is severely curtailed in females with Rett syndrome

Rett syndrome (RTT), a rare neurodevelopmental disorder caused by mutations in the MECP2 gene, is typified by profound cognitive impairment and severe language impairment, rendering it very difficult to accurately measure auditory processing capabilities behaviorally in this population. Here we leve...

Descripción completa

Detalles Bibliográficos
Autores principales: Brima, Tufikameni, Molholm, Sophie, Molloy, Ciara J., Sysoeva, Olga V., Nicholas, Eric, Djukic, Aleksandra, Freedman, Edward G., Foxe, John J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6456588/
https://www.ncbi.nlm.nih.gov/pubmed/30967526
http://dx.doi.org/10.1038/s41398-019-0463-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6456588/
https://www.ncbi.nlm.nih.gov/pubmed/30967526
http://dx.doi.org/10.1038/s41398-019-0463-0

Ejemplares similares