Deficits in skilled motor and auditory learning in a rat model of Rett syndrome

BACKGROUND: Rett syndrome is an X-linked neurodevelopmental disorder caused by a mutation in the gene MECP2. Individuals with Rett syndrome display developmental regression at an early age, and develop a range of motor, auditory, cognitive, and social impairments. Several studies have successfully m...

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Detalles Bibliográficos
Autores principales: Adcock, Katherine S., Blount, Abigail E., Morrison, Robert A., Alvarez-Dieppa, Amanda, Kilgard, Michael P., Engineer, Crystal T., Hays, Seth A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7523346/
https://www.ncbi.nlm.nih.gov/pubmed/32988374
http://dx.doi.org/10.1186/s11689-020-09330-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7523346/
https://www.ncbi.nlm.nih.gov/pubmed/32988374
http://dx.doi.org/10.1186/s11689-020-09330-5

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