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Article

Retrospective mutational analysis of NPHS1, NPHS2, WT1 and LAMB2 in children with steroid-resistant focal segmental glomerulosclerosis - a single-centre experience.

Bosnian journal of basic medical sciences - 1 May 2014

Bińczak-Kuleta Agnieszka, Rubik Jacek, Litwin Mieczysław, Ryder Małgorzata, Lewandowska Klaudyna, Taryma-Leśniak Olga, Clark Jeremy S, Grenda Ryszard, Ciechanowicz Andrzej

Abstract excerpt

The aim of our study was to examine NPHS1, NPHS2, WT1 and LAMB2 mutations, previously reported in two thirds of patients with nephrotic syndrome with onset before the age of one year old. Genomic DNA samples from Polish children (n=33) with Steroid-Resistant Nephrotic Syndrome (SRNS) due to focal segmental glomerulosclerosis (FSGS), manifesting before the age of 13 years old, underwent retrospective analysis of...

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Source

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Identifiers

PMID: 24856380
DOI: 10.17305/bjbms.2014.2270
PMCID: PMC4333957

Genes

NPHS2
LAMB2
NPHS1

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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