Functional, structural, and metabolic abnormalities of the hippocampal formation in Williams syndrome

Williams syndrome (WS), caused by microdeletion of some 21 genes on chromosome 7q11.23, is characterized by dysmorphic features, mental retardation or learning difficulties, elastin arteriopathy, and striking neurocognitive and social-behavioral abnormalities. Recent studies of murine knockouts of k...

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Main Authors: Meyer-Lindenberg, Andreas, Mervis, Carolyn B., Sarpal, Deepak, Koch, Paul, Steele, Sonya, Kohn, Philip, Marenco, Stefano, Morris, Colleen A., Das, Saumitra, Kippenhan, Shane, Mattay, Venkata S., Weinberger, Daniel R., Berman, Karen Faith
Formato: Artigo
Idioma:Inglês
Publicado: American Society for Clinical Investigation 2005
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Research Article
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC1143592/
https://ncbi.nlm.nih.gov/pubmed/15951840
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI24892
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