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Essential Roles for ARID1B in Dendritic Arborization and Spine Morphology of Developing Pyramidal Neurons
De novo truncating mutations in ARID1B, a chromatin-remodeling gene, cause Coffin–Siris syndrome, a developmental disorder characterized by intellectual disability and speech impairment; however, how the genetic elimination leads to cognitive dysfunction remains unknown. Thus, we investigated the ne...
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Publicado no: | J Neurosci |
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Main Authors: | , , , |
Formato: | Artigo |
Idioma: | Inglês |
Publicado em: |
Society for Neuroscience
2016
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Assuntos: | |
Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4879215/ https://ncbi.nlm.nih.gov/pubmed/26937011 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.2321-15.2016 |
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