ロード中...
Fragile X syndrome: Mechanistic insights and therapeutic avenues regarding the role of potassium channels
Fragile X syndrome (FXS) is a common form of mental disability and one of the known causes of autism. The mutation responsible for FXS is a large expansion of the trinucleotide CGG repeats which leads to DNA methylation of the fragile X mental retardation gene 1 (FMR1) and transcriptional silencing,...
保存先:
| 主要な著者: | , |
|---|---|
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
2012
|
| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3393774/ https://ncbi.nlm.nih.gov/pubmed/22483378 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.conb.2012.03.010 |
| 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!
|