Associated Papers
Mutations in UMOD Contribute to the Pathogenesis of ADTKD-UMOD by Influencing the Function of Complement Factor H.
Xie Q et al.
Journal of Cellular and Molecular Medicine, 2026
Implementation of a Kidney Genetic Service Into the Diagnostic Pathway for Patients With Chronic Kidney Disease in Canada.
Schott C et al.
Kidney International Reports, 2025
39990878 (PubMed )
Supplement: mmc1.pdf
Autosomal dominant tubulointerstitial kidney disease genotype and phenotype correlation in a Chinese cohort.
Gong K et al.
Scientific Reports, 2021
UMOD gene mutations in Chinese patients with autosomal dominant tubulointerstitial kidney disease: a pediatric case report and literature review.
Yang J et al.
Bmc Pediatrics, 2019
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