SHANK2 mutations associated with Autism Spectrum Disorder cause hyperconnectivity of human neurons

Heterozygous loss-of-function mutations in SHANK2 are associated with autism spectrum disorder (ASD). We generated cortical neurons from induced pluripotent stem cells (iPSC) derived from neurotypic and ASD-affected donors. We developed Sparse coculture for Connectivity (SparCon) assays where SHANK2...

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Detalles Bibliográficos
Autores principales: Zaslavsky, Kirill, Zhang, Wen-Bo, McCready, Fraser P., Rodrigues, Deivid C., Deneault, Eric, Loo, Caitlin, Zhao, Melody, Ross, P. Joel, Hajjar, Joelle El, Romm, Asli, Thompson, Tadeo, Piekna, Alina, Wei, Wei, Wang, Zhuozhi, Khattak, Shahryar, Mufteev, Marat, Pasceri, Peter, Scherer, Stephen W., Salter, Michael W., Ellis, James
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6475597/
https://www.ncbi.nlm.nih.gov/pubmed/30911184
http://dx.doi.org/10.1038/s41593-019-0365-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6475597/
https://www.ncbi.nlm.nih.gov/pubmed/30911184
http://dx.doi.org/10.1038/s41593-019-0365-8

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