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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...
| Autores principales: | , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Cell Press
2017
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| Materias: | |
| 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 |