Associated Papers
From mutation to symptoms: a multi-center study on HNF1B-related nephropathy in Chinese children.
Zhang H et al.
Bmc Nephrology, 2025
Genetic spectrum of CAKUT and risk factors for kidney failure: a pediatric multicenter cohort study.
Liu JL et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association, 2022
36549658 (PubMed )
Supplement: gfac338_supplemental_file.pdf
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