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Molecular analyses of neurogenic defects in a human pluripotent stem cell model of fragile X syndrome

New research suggests that common pathways are altered in many neurodevelopmental disorders including autism spectrum disorder; however, little is known about early molecular events that contribute to the pathology of these diseases. The study of monogenic, neurodevelopmental disorders with a high i...

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Detalhes bibliográficos
Publicado no:Brain
Main Authors: Boland, Michael J., Nazor, Kristopher L., Tran, Ha T., Szücs, Attila, Lynch, Candace L., Paredes, Ryder, Tassone, Flora, Sanna, Pietro Paolo, Hagerman, Randi J., Loring, Jeanne F.
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2017
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5837342/
https://ncbi.nlm.nih.gov/pubmed/28137726
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/brain/aww357
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