Resting State Functional Connectivity Is Decreased Globally Across the C9orf72 Mutation Spectrum

A repeat expansion mutation in the C9orf72 gene causes amyotrophic lateral sclerosis (ALS), frontotemporal dementia (FTD), or symptoms of both, and has been associated with gray and white matter changes in brain MRI scans. We used graph theory to examine the network properties of brain function at r...

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Detalles Bibliográficos
Autores principales: Smallwood Shoukry, Rachel F., Clark, Michael G., Floeter, Mary Kay
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Neurology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7710968/
https://www.ncbi.nlm.nih.gov/pubmed/33329355
http://dx.doi.org/10.3389/fneur.2020.598474

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7710968/
https://www.ncbi.nlm.nih.gov/pubmed/33329355
http://dx.doi.org/10.3389/fneur.2020.598474

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