載入...
APOL1 polymorphisms and kidney disease: loss-of-function or gain-of-function?
The mechanism that explains the association of APOL1 variants with nondiabetic kidney diseases in African Americans remains unclear. Kidney disease risk is inherited as a recessive trait, and many studies investigating the intracellular function of APOL1 have indicated the APOL1 variants G1 and G2 a...
Na minha lista:
| 發表在: | Am J Physiol Renal Physiol |
|---|---|
| Main Authors: | , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
American Physiological Society
2019
|
| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6383195/ https://ncbi.nlm.nih.gov/pubmed/30332315 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1152/ajprenal.00426.2018 |
| 標簽: |
添加標簽
沒有標簽, 成為第一個標記此記錄!
|