ロード中...
Progranulin mutations result in impaired processing of prosaposin and reduced glucocerebrosidase activity
Frontotemporal dementia (FTD) is a common neurogenerative disorder characterized by progressive degeneration in the frontal and temporal lobes. Heterozygous mutations in the gene encoding progranulin (PGRN) are a common genetic cause of FTD. Recently, PGRN has emerged as an important regulator of ly...
保存先:
| 出版年: | Hum Mol Genet |
|---|---|
| 主要な著者: | , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Oxford University Press
2020
|
| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7104673/ https://ncbi.nlm.nih.gov/pubmed/31600775 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddz229 |
| 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!
|