ロード中...
Aquaporin-2: new mutations responsible for autosomal-recessive nephrogenic diabetes insipidus—update and epidemiology
It is clinically useful to distinguish between two types of hereditary nephrogenic diabetes insipidus (NDI): a ‘pure’ type characterized by loss of water only and a complex type characterized by loss of water and ions. Patients with congenital NDI bearing mutations in the vasopressin 2 receptor gene...
保存先:
| 出版年: | Clin Kidney J |
|---|---|
| 主要な著者: | , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Oxford University Press
2012
|
| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4400507/ https://ncbi.nlm.nih.gov/pubmed/26069764 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/ckj/sfs029 |
| 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!
|