Late onset of familial nephrotic syndrome associated with a compound heterozygous mutation of the podocin-encoding gene (Case Report)
Author:
Publisher
Wiley
Subject
Nephrology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1440-1797.2005.00481.x/fullpdf
Reference11 articles.
1. Mutations in NPHS2 Encoding Podocin Are a Prevalent Cause of Steroid-Resistant Nephrotic Syndrome among Israeli-Arab Children
2. In situ evaluation of podocin in normal and glomerular diseases
3. NPHS2 mutation analysis shows genetic heterogeneityof steroid-resistant nephrotic syndrome and lowpost-transplant recurrence
4. A Mutation in the TRPC6 Cation Channel Causes Familial Focal Segmental Glomerulosclerosis
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2. Clinical and pathological phenotype of genetic causes of focal segmental glomerulosclerosis in adults;Clinical Kidney Journal;2018-01-09
3. Identificación de variantes del gen NPHS2 en niños con síndrome nefrótico corticorresistente;Revista Chilena de Pediatría;2016-01
4. The amino acid mutations of the podocin in proteinuria: a meta-analysis;Renal Failure;2015-07-27
5. Clinical Value ofNPHS2Analysis in Early- and Adult-Onset Steroid-Resistant Nephrotic Syndrome;Clinical Journal of the American Society of Nephrology;2010-10-14
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