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Metabolic Changes in Polycystic Kidney Disease as a Potential Target for Systemic Treatment
Autosomal recessive and autosomal dominant polycystic kidney disease (ARPKD, ADPKD) are systemic disorders with pronounced hepatorenal phenotypes. While the main underlying genetic causes of both ARPKD and ADPKD have been well-known for years, the exact molecular mechanisms resulting in the observed...
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| Udgivet i: | Int J Mol Sci |
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| Main Authors: | , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
MDPI
2020
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7503958/ https://ncbi.nlm.nih.gov/pubmed/32847032 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms21176093 |
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