Nipbl Interacts with Zfp609 and the Integrator Complex to Regulate Cortical Neuron Migration

Mutations in NIPBL are the most frequent cause of Cornelia de Lange syndrome (CdLS), a developmental disorder encompassing several neurological defects, including intellectual disability and seizures. How NIPBL mutations affect brain development is not understood. Here we identify Nipbl as a functio...

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Detalles Bibliográficos
Autores principales: van den Berg, Debbie L.C., Azzarelli, Roberta, Oishi, Koji, Martynoga, Ben, Urbán, Noelia, Dekkers, Dick H.W., Demmers, Jeroen A., Guillemot, François
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2017
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5263256/
https://www.ncbi.nlm.nih.gov/pubmed/28041881
http://dx.doi.org/10.1016/j.neuron.2016.11.047

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5263256/
https://www.ncbi.nlm.nih.gov/pubmed/28041881
http://dx.doi.org/10.1016/j.neuron.2016.11.047

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