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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Publicat a:Nature
Autors principals: 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.
Format: Artigo
Idioma:Inglês
Publicat: 2016
Matèries:
Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4995142/
https://ncbi.nlm.nih.gov/pubmed/27509850
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/nature19067
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