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3. Renal and Extrarenal Phenotypes in Patients With HNF1B Variants and Chromosome 17q12 Microdeletions

4. The genetic landscape and clinical spectrum of nephronophthisis and related ciliopathies

5. Benign and malignant proliferation in idiopathic nephrotic syndrome: a French cohort study

6. Results from a nationwide retrospective cohort measure the impact of C3 and soluble C5b-9 levels on kidney outcomes in C3 glomerulopathy

7. Corrigendum: Human C-terminal CUBN variants associate with chronic proteinuria and normal renal function

9. Human C-terminal CUBN variants associate with chronic proteinuria and normal renal function

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