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Age at diagnosis of NS in correlation to detected pathogenic mutations in NPHS1, NPHS2, WT1, TRPC6, and INF2 in 110 families (we did not include the ACTN4 and CD2AP genes because no pathogenic mutations were identified in our cohort). (A) Familial and sporadic cases. (B) Percentage of mutations in familial cases. (C) Percentage of mutations in sporadic cases.
