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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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| Publicat a: | J Neurodev Disord |
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| Autors principals: | , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BioMed Central
2020
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7523346/ https://ncbi.nlm.nih.gov/pubmed/32988374 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s11689-020-09330-5 |
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