ロード中...
Loss of TMEM106B potentiates lysosomal and FTLD‐like pathology in progranulin‐deficient mice
Single nucleotide polymorphisms (SNPs) in TMEM106B encoding the lysosomal type II transmembrane protein 106B increase the risk for frontotemporal lobar degeneration (FTLD) of GRN (progranulin gene) mutation carriers. Currently, it is unclear if progranulin (PGRN) and TMEM106B are synergistically lin...
保存先:
| 出版年: | EMBO Rep |
|---|---|
| 主要な著者: | , , , , , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
John Wiley and Sons Inc.
2020
|
| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7534633/ https://ncbi.nlm.nih.gov/pubmed/32929860 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.15252/embr.202050241 |
| 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!
|