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Abnormal Network Activity in a Targeted Genetic Model of Human Double Cortex
In human patients, cortical dysplasia produced by Doublecortin (DCX) mutations lead to mental retardation and intractable infantile epilepsies, but the underlying mechanisms are not known. DCX(−/−) mice have been generated to investigate this issue. However, they display no neocortical abnormality,...
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| Publicado en: | J Neurosci |
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| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Society for Neuroscience
2009
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6664957/ https://ncbi.nlm.nih.gov/pubmed/19144832 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.4093-08.2009 |
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