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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Bibliografski detalji
Izdano u:J Neurosci
Glavni autori: Ackman, James B., Aniksztejn, Laurent, Crépel, Valérie, Becq, Hélène, Pellegrino, Christophe, Cardoso, Carlos, Ben-Ari, Yehezkel, Represa, Alfonso
Format: Artigo
Jezik:Inglês
Izdano: Society for Neuroscience 2009
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Articles
Online pristup: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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