ロード中...
Novel SLC5A2 mutation contributes to familial renal glucosuria: Abnormal expression in renal tissues
Familial renal glucosuria (FRG) is characterized by persistent glucosuria in the presence of normal serum glucose concentrations, while other impairments of tubular function are absent. Mutations in the sodium-glucose co-transporter 2 (SLC5A2) gene have been found to be responsible for FRG. However,...
保存先:
| 出版年: | Exp Ther Med |
|---|---|
| 主要な著者: | , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
D.A. Spandidos
2016
|
| 主題: | |
| オンライン・アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4950299/ https://ncbi.nlm.nih.gov/pubmed/27446256 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/etm.2016.3388 |
| 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!
|