ロード中...
Altered cortical Cytoarchitecture in the Fmr1 knockout mouse
Fragile X syndrome (FXS) is a neurodevelopmental disorder caused by silencing of the FMR1 gene and subsequent loss of its protein product, fragile X retardation protein (FMRP). One of the most robust neuropathological findings in post-mortem human FXS and Fmr1 KO mice is the abnormal increase in den...
保存先:
| 出版年: | Mol Brain |
|---|---|
| 主要な著者: | , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
BioMed Central
2019
|
| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6570929/ https://ncbi.nlm.nih.gov/pubmed/31200759 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13041-019-0478-8 |
| 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!
|