| License: Creative Commons Attribution 4.0 PDF - Published Version (9MB) |
- URN to cite this document:
- urn:nbn:de:bvb:355-epub-770006
- DOI to cite this document:
- 10.5283/epub.77000
This publication is part of the DEAL contract with Springer.
Abstract
Background Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary kidney disorder characterized by progressive renal cyst formation, often leading to end-stage kidney disease (ESKD). In contrast to the urinary metabolome in ADPKD, the composition of renal cyst fluid remains largely unexplored. Methods We conducted a comprehensive metabolomic analysis of renal cyst ...

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