Resting state functional MRI reveals abnormal network connectivity in neurofibromatosis 1

Neurofibromatosis type I (NF1) is a genetic disorder caused by mutations in the neurofibromin 1 gene at locus 17q11.2. Individuals with NF1 have an increased incidence of learning disabilities, attention deficits, and autism spectrum disorders. As a single‐gene disorder, NF1 represents a valuable mo...

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Vydáno v:Hum Brain Mapp
Hlavní autoři: Tomson, Steffie N., Schreiner, Matthew J., Narayan, Manjari, Rosser, Tena, Enrique, Nicole, Silva, Alcino J., Allen, Genevera I., Bookheimer, Susan Y., Bearden, Carrie E.
Médium: Artigo
Jazyk:Inglês
Vydáno: John Wiley and Sons Inc. 2015
Témata:
Research Articles
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4619152/
https://ncbi.nlm.nih.gov/pubmed/26304096
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/hbm.22937
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