Whole-genome sequencing reveals contribution of rare and common variation to structural kidney and urinary tract malformations

Zenodo (CERN European Organization for Nuclear Research) 2026 Dataset Open access

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Authors: Melanie Chan
DOI: 10.5281/zenodo.18040141
Cited by: 0

Abstract

Supplementary tables detailing analysis of whole-genome sequencing data from 1,052 patients with congenital anomalies of the kidneys and urinary tract (CAKUT).

Publication details

Journal / source
Zenodo (CERN European Organization for Nuclear Research)
Publication date
5 January 2026
Document type
Dataset