An affected core drives network integration deficits of the structural connectome in 22q11.2 deletion syndrome

Chromosome 22q11.2 deletion syndrome (22q11DS) is a genetic disease known to lead to cerebral structural alterations, which we study using the framework of the macroscopic white-matter connectome. We create weighted connectomes of 44 patients with 22q11DS and 44 healthy controls using diffusion tens...

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Detalles Bibliográficos
Autores principales: Váša, František, Griffa, Alessandra, Scariati, Elisa, Schaer, Marie, Urben, Sébastien, Eliez, Stephan, Hagmann, Patric
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Regular Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4711395/
https://www.ncbi.nlm.nih.gov/pubmed/26870660
http://dx.doi.org/10.1016/j.nicl.2015.11.017

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4711395/
https://www.ncbi.nlm.nih.gov/pubmed/26870660
http://dx.doi.org/10.1016/j.nicl.2015.11.017

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