Williams syndrome hemideletion and LIMK1 variation both affect dorsal stream functional connectivity.

Williams syndrome is a rare genetic disorder caused by hemizygous deletion of ∼1.6 Mb affecting 26 genes on chromosome 7 (7q11.23) and is clinically typified by two cognitive/behavioural hallmarks: marked visuospatial deficits relative to verbal and non-verbal reasoning abilities and hypersocial per...

Descripción completa

Detalles Bibliográficos

Publicado en:	Brain: A Journal of Neurology Vol. 142; no. 12; pp. 3963 - 3975
Autores principales:	Gregory, Michael D, Mervis, Carolyn B, Elliott, Maxwell L, Kippenhan, J Shane, Nash, Tiffany, Czarapata, Jasmin B., Prabhakaran, Ranjani, Roe, Katherine, Eisenberg, Daniel P, Kohn, Philip D, Berman, Karen F, B Czarapata, Jasmin
Formato:	research Journal Article
Publicado:	Oxford University Press / USA Dec2019
Acceso en línea:	Ver este registro en EBSCOhost