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...

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Detalles Bibliográficos
Autores principales: Shofty, Ben, Bergmann, Eyal, Zur, Gil, Asleh, Jad, Bosak, Noam, Kavushansky, Alexandra, Castellanos, F. Xavier, Ben-Sira, Liat, Packer, Roger J., Vezina, Gilbert L., Constantini, Shlomi, Acosta, Maria T., Kahn, Itamar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2019
Materias:
Article
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

Internet

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

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