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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Detalhes bibliográficos
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 em: American Society for Clinical Investigation 2005
Assuntos:
Research Article
Acesso em linha: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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