A human neurodevelopmental model for Williams syndrome

Williams syndrome (WS) is a genetic neurodevelopmental disorder characterized by an uncommon hypersociability and a mosaic of retained and compromised linguistic and cognitive abilities. Nearly all clinically diagnosed individuals with WS lack precisely the same set of genes, with breakpoints in chr...

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Detalles Bibliográficos
Autores principales: Chailangkarn, Thanathom, Trujillo, Cleber A., Freitas, Beatriz C., Hrvoj-Mihic, Branka, Herai, Roberto H., Yu, Diana X., Brown, Timothy T., Marchetto, Maria C. N., Bardy, Cedric, McHenry, Lauren, Stefanacci, Lisa, Järvinen, Anna, Searcy, Yvonne M., DeWitt, Michelle, Wong, Wenny, Lai, Philip, Ard, M. Colin, Hanson, Kari L., Romero, Sarah, Jacobs, Bob, Dale, Anders M., Dai, Li, Korenberg, Julie R., Gage, Fred H., Bellugi, Ursula, Halgren, Eric, Semendeferi, Katerina, Muotri, Alysson R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2016
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4995142/
https://www.ncbi.nlm.nih.gov/pubmed/27509850
http://dx.doi.org/10.1038/nature19067

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4995142/
https://www.ncbi.nlm.nih.gov/pubmed/27509850
http://dx.doi.org/10.1038/nature19067

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