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...

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Detalhes bibliográficos
Main Authors: 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
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2009
Assuntos:
Original Articles
Acesso em linha: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
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