2000•Kidney InternationalOpen access

Congenital nephrotic syndrome (NPHS1): Features resulting from different mutations in Finnish patients

Jaakko Patrakka, Marjo Kestilä, Jorma Wartiovaara, Vesa Ruotsalainen, Päivi Tissari, Ulla Lenkkeri, Minna Männikkö, Ilona Visapää, Christer Holmberg, Juhani Rapola, Karl Tryggvason, Hannu Jalanko

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Key concepts: Nephrin, Congenital nephrotic syndrome, Slit diaphragm, Podocyte, Nephrotic syndrome, Focal segmental glomerulosclerosis, Genotype, Biology

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Congenital nephrotic syndrome (NPHS1): Features resulting from different mutations in Finnish patients — Research Paper | ScholarLens