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Autism-associated Nf1 deficiency disrupts corticocortical and corticostriatal functional connectivity in human and mouse
Children with the autosomal dominant single gene disorder, neurofibromatosis type 1 (NF1), display multiple structural and functional changes in the central nervous system, resulting in neuropsychological cognitive abnormalities. Here we assessed the pathological functional organization that may und...
| Autores principales: | , , , , , , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
2019
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6689441/ https://www.ncbi.nlm.nih.gov/pubmed/31128207 http://dx.doi.org/10.1016/j.nbd.2019.104479 |