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APOL1 and mechanisms of kidney disease susceptibility
PURPOSE OF REVIEW: Allelic variants in the gene for apolipoprotein L1 (APOL1), found only in individuals of African ancestry, explain a majority of the excess risk of kidney disease in African Americans. However, a clear understanding how the disease-associated APOL1 variants cause kidney injury and...
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| Gepubliceerd in: | Curr Opin Nephrol Hypertens |
|---|---|
| Hoofdauteurs: | , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
2021
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8211384/ https://ncbi.nlm.nih.gov/pubmed/33767059 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/MNH.0000000000000704 |
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