Published January 5, 2026
| Version v2
Dataset
Open
Whole-genome sequencing reveals contribution of rare and common variation to structural kidney and urinary tract malformations
Authors/Creators
- 1. Imperial College London
-
2.
University College London
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3.
MRC London Institute of Medical Sciences
Description
Supplementary tables detailing analysis of whole-genome sequencing data from 1,052 patients with congenital anomalies of the kidneys and urinary tract (CAKUT).
Files
bladderexstrophy_10e4_lof_missense_genes.txt
Files
(6.7 GB)
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