ロード中...
Global Gene Expression Profiling in R155H Knock‐In Murine Model of VCP Disease
Dominant mutations in the valosin‐containing protein (VCP) gene cause inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia, which is characterized by progressive muscle weakness, dysfunction in bone remodeling, and frontotemporal dementia. More recently, VCP has...
保存先:
| 出版年: | Clin Transl Sci |
|---|---|
| 主要な著者: | , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
John Wiley and Sons Inc.
2014
|
| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4329058/ https://ncbi.nlm.nih.gov/pubmed/25388089 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/cts.12241 |
| 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!
|