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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...
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| Publicat a: | Transl Psychiatry |
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| Autors principals: | , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Nature Publishing Group UK
2019
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6456588/ https://ncbi.nlm.nih.gov/pubmed/30967526 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41398-019-0463-0 |
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