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Limbic Epileptogenesis in a Mouse Model of Fragile X Syndrome
Fragile X syndrome (FXS), caused by silencing of the Fmr1 gene, is the most common form of inherited mental retardation. Epilepsy is reported to occur in 20–25% of individuals with FXS. However, no overall increased excitability has been reported in Fmr1 knockout (KO) mice, except for increased sens...
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| 主要な著者: | , , , , , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Oxford University Press
2009
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2693616/ https://ncbi.nlm.nih.gov/pubmed/18832330 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/cercor/bhn163 |
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