ロード中...
Loss of MeCP2 From Forebrain Excitatory Neurons Leads to Cortical Hyperexcitation and Seizures
Mutations of MECP2 cause Rett syndrome (RTT), a neurodevelopmental disorder leading to loss of motor and cognitive functions, impaired social interactions, and seizure at young ages. Defects of neuronal circuit development and function are thought to be responsible for the symptoms of RTT. The major...
保存先:
| 主要な著者: | , , , , |
|---|---|
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Society for Neuroscience
2014
|
| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3921436/ https://ncbi.nlm.nih.gov/pubmed/24523563 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.4900-12.2014 |
| タグ: |
タグ追加
タグなし, このレコードへの初めてのタグを付けませんか!
|