Retinotopically defined primary visual cortex in Williams syndrome

Williams syndrome, caused by a hemizygous microdeletion on chromosome 7q11.23, is characterized by severe impairment in visuospatial construction. To examine potential contributions of early visual processing to this cognitive problem, we functionally mapped the size and neuroanatomical variability...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: Olsen, Rosanna K., Kippenhan, J. Shane, Japee, Shruti, Kohn, Philip, Mervis, Carolyn B., Saad, Ziad S., Morris, Colleen A., Meyer-Lindenberg, Andreas, Berman, Karen Faith
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Oxford University Press 2009
Pynciau:
Original Articles
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC2724925/
https://ncbi.nlm.nih.gov/pubmed/19255058
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/brain/awn362
Tagiau: Ychwanegu Tag
Dim Tagiau, Byddwch y cyntaf i dagio'r cofnod hwn!

Eitemau Tebyg