Article info
Developmental defects
Short report
Autosomal dominant polycystic kidney disease in absence of renal cyst formation illustrates genetic interaction between WT1 and PKD1
- Correspondence to Dr Jan Halbritter, Division of Nephrology, Department of Internal Medicine, Leipzig University, 04109 Leipzig, Saxony, Germany; jan.halbritter{at}medizin.uni-leipzig.de
Citation
Autosomal dominant polycystic kidney disease in absence of renal cyst formation illustrates genetic interaction between WT1 and PKD1
Publication history
- Received October 15, 2019
- Revised March 5, 2020
- Accepted March 20, 2020
- First published May 7, 2020.
Online issue publication
January 22, 2021
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- Previous version (16 June 2020).
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© Author(s) (or their employer(s)) 2021. No commercial re-use. See rights and permissions. Published by BMJ.