ロード中...
Lysozyme amyloidosis – a case report and review of the literature
Lysozyme amyloidosis is an exceedingly rare hereditary autosomal dominant amyloidosis, which is characterized by the precipitation of lysozyme protein within the body, leading to multi-organ dysfunction. Herein, we present the case of a U.S. family affected by lysozyme amyloidosis. In particular, we...
保存先:
| 出版年: | Clin Nephrol Case Stud |
|---|---|
| 主要な著者: | , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Dustri-Verlag Dr. Karl Feistle
2015
|
| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5437999/ https://ncbi.nlm.nih.gov/pubmed/29043133 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5414/CNCS108538 |
| 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!
|