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Query Trace: Proteinuria and ACTN4[original query]

Screening of ACTN4 and TRPC6 mutations in a Chinese cohort of patients with adult-onset familial focal segmental glomerulosclerosis. Contributions to nephrology 2013 181 91-100. Zhang Qianying, Ma Jun, Xie Jingyuan, Wang Zhaohui, Zhu Bin, Hao Xu, Yang Li, Ren Hong, Chen N Similar articles in PubMed
The R229Q mutation in NPHS2 may predispose to proteinuria in thin-basement-membrane nephropathy. Pediatric nephrology (Berlin, Germany) 2008 Dec 23 (12): 2201-7. Tonna Stephen, Wang Yan Yan, Wilson Diane, Rigby Lin, Tabone Tania, Cotton Richard, Savige Ju Similar articles in PubMed
Association analysis of podocyte slit diaphragm genes as candidates for diabetic nephropathy. Diabetologia 2008 Jan 51 (1): 86-90. Ihalmo P, Wessman M, Kaunisto M A, Kilpikari R, Parkkonen M, Forsblom C, Holthöfer H, Groop P-H, Similar articles in PubMed
Molecular analysis of NPHS2 and ACTN4 genes in a series of 33 Italian patients affected by adult-onset nonfamilial focal segmental glomerulosclerosis. Nephron. Clinical practice 2005 1 99 (2): c31-6. Aucella Filippo, De Bonis Patrizia, Gatta Giuseppe, Muscarella Lucia Anna, Vigilante Mimmo, di Giorgio Giuseppe, D'Errico Michele, Zelante Leopoldo, Stallone Carmine, Bisceglia Lui Similar articles in PubMed