ロード中...
A novel deletion in the RCA gene cluster causes atypical hemolytic uremic syndrome
Atypical hemolytic uremic syndrome (aHUS) is a complex complement-mediated disease that progresses to end-stage renal failure (ESRF) in 50% of cases. Dysregulation of the alternative pathway (AP) of the complement cascade manifests as microangiopathic anaemia and thrombocytopenia. Multiple genes in...
保存先:
| 出版年: | Nephrol Dial Transplant |
|---|---|
| 主要な著者: | , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Oxford University Press
2011
|
| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6937010/ https://ncbi.nlm.nih.gov/pubmed/20974643 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/ndt/gfq658 |
| 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!
|