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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Autors principals: 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
Format: Artigo
Idioma:Inglês
Publicat: American Society for Clinical Investigation 2005
Matèries:
Research Article
Accés en línia: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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