Associated Papers
Unprecedented coexistence of Dent's disease type 1 and Wilson's disease in a two-year-old Chinese boy: implications for precision medicine.
Mao Q et al.
Bmc Nephrology, 2025
Genotype-Phenotype Correlation Reanalysis in 83 Chinese Cases with OCRL Mutations.
Zhang L et al.
Genetics Research, 2022
Genotype Phenotype Correlation in Dent Disease 2 and Review of the Literature: OCRL Gene Pleiotropism or Extreme Phenotypic Variability of Lowe Syndrome?
Gianesello L et al.
Genes, 2021
Genetics and phenotypic heterogeneity of Dent disease: the dark side of the moon.
Gianesello L et al.
Human Genetics, 2021
32860533 (PubMed )
Supplement: 439_2020_2219_MOESM1_ESM.docx
Phenotypic spectrum and antialbuminuric response to angiotensin converting enzyme inhibitor and angiotensin receptor blocker therapy in pediatric Dent disease.
Deng H et al.
Molecular Genetics & Genomic Medicine, 2020
Dent's disease complicated by nephrotic syndrome: A case report.
He G et al.
Intractable & Rare Diseases Research, 2016
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