A Genetic Model for Understanding Higher Order Visual Processing: Functional Interactions of the Ventral Visual Stream in Williams Syndrome

Williams syndrome (WS) is a rare neurodevelopmental disorder caused by a 1.6 Mb microdeletion on chromosome 7q11.23 and characterized by hypersocial personality and prominent visuospatial construction impairments. Previous WS studies have identified functional and structural abnormalities in the hip...

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Hauptverfasser: Sarpal, Deepak, Buchsbaum, Bradley R., Kohn, Philip D., Kippenhan, J. Shane, Mervis, Carolyn B., Morris, Colleen A., Meyer-Lindenberg, Andreas, Berman, Karen Faith
Format: Artigo
Sprache:Inglês
Veröffentlicht: Oxford University Press 2008
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Articles
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC2733313/
https://ncbi.nlm.nih.gov/pubmed/18308711
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/cercor/bhn004
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