Visual phenotype in Williams-Beuren syndrome challenges magnocellular theories explaining human neurodevelopmental visual cortical disorders

Williams-Beuren syndrome (WBS), a neurodevelopmental genetic disorder whose manifestations include visuospatial impairment, provides a unique model to link genetically determined loss of neural cell populations at different levels of the nervous system with neural circuits and visual behavior. Given...

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Detalhes bibliográficos
Main Authors: Castelo-Branco, Miguel, Mendes, Mafalda, Sebastião, Ana Raquel, Reis, Aldina, Soares, Mário, Saraiva, Jorge, Bernardes, Rui, Flores, Raquel, Pérez-Jurado, Luis, Silva, Eduardo
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Clinical Investigation 2007
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Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2082146/
https://ncbi.nlm.nih.gov/pubmed/18037993
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI32556
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