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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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| Hoofdauteurs: | , , , , , , , , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Oxford University Press
2009
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| Onderwerpen: | |
| Online toegang: | 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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