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3. Rare variants in tenascin genes in a cohort of children with primary vesicoureteric reflux

4. HLA-DQA1 and PLCG2 Are Candidate Risk Loci for Childhood-Onset Steroid-Sensitive Nephrotic Syndrome

5. A Novel Missense Mutation of Wilms’ Tumor 1 Causes Autosomal Dominant FSGS

6. Rare hereditary COL4A3/COL4A4 variants may be mistaken for familial focal segmental glomerulosclerosis

7. Mutations in the Gene That Encodes the F-Actin Binding Protein Anillin Cause FSGS

8. Phosphodiesterase 5 inhibition ameliorates angiontensin II-induced podocyte dysmotility via the protein kinase G-mediated downregulation of TRPC6 activity

9. TNXB Mutations Can Cause Vesicoureteral Reflux

10. Inverted formin 2 mutations with variable expression in patients with sporadic and hereditary focal and segmental glomerulosclerosis

11. TRPC6 Enhances Angiotensin II-induced Albuminuria

12. A New Locus for Familial FSGS on Chromosome 2P

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