Extensive characterization of a Williams Syndrome murine model shows Gtf2ird1-mediated rescue of select sensorimotor tasks, but no effect on enhanced social behavior

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Williams Syndrome is a rare neurodevelopmental disorder exhibiting cognitive and behavioral abnormalities, including increased social motivation, risk of anxiety and specific phobias along with perturbed motor function. Williams Syndrome is caused by a microdeletion of 26–28 genes on chromosome 7, i...

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Detalles Bibliográficos
Autores principales: Nygaard, Kayla R., Maloney, Susan E., Swift, Raylynn G., McCullough, Katherine B., Wagner, Rachael E., Fass, Stuart B., Garbett, Krassimira, Mirnics, Karoly, Veenstra-VanderWeele, Jeremy, Dougherty, Joseph D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9882309/
https://www.ncbi.nlm.nih.gov/pubmed/36711815
http://dx.doi.org/10.1101/2023.01.18.523029

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9882309/
https://www.ncbi.nlm.nih.gov/pubmed/36711815
http://dx.doi.org/10.1101/2023.01.18.523029

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