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29. Thirteen novel NPHS1 mutations in a large cohort of children with congenital nephrotic syndrome. Heeringa SF, Vlangos CN, Chernin G, Hinkes B, Gbadegesin R, Liu J, Hoskins BE, Ozaltin F, Hildebrandt F, Members of the APN Study Group. Nephrol Dial Transplant; 2008 Nov; 23(11):3527-33. PubMed ID: 18503012 [Abstract] [Full Text] [Related]
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