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Heterozygous Dab1 Null Mutation Disrupts Neocortical and Hippocampal Development
Loss-of-function mutations in Reelin and DAB1 signaling pathways disrupt proper neuronal positioning in the cerebral neocortex and hippocampus, but the underlying molecular mechanisms remain elusive. Here, we report that heterozygous yotari mice harboring a single autosomal recessive yotari mutation...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Society for Neuroscience
2023
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10089055/ https://www.ncbi.nlm.nih.gov/pubmed/36941061 http://dx.doi.org/10.1523/ENEURO.0433-22.2023 |