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Article

NPHS2 variation in Chinese southern infants with late steroid-resistant nephrotic syndrome.

Renal failure - 1 Oct 2014

Dai Yiheng, Yang Hui, Gao Pingming, Liu Wei Dong

Abstract excerpt

Abstract NPHS2 mutations are responsible for autosomal recessive familial steroid-resistant nephrotic syndrome (SRNS) with minor glomerular abnormalities or focal segmental glomerulosclerosis (FSGS), which is characterized by early childhood onset and rapid progression to chronic renal insufficiency. This gene mutation is also responsible for an adolescent onset form of autosomal recessive familial FSGS with...

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Identifiers

PMID: 25112471
DOI: 10.3109/0886022X.2014.947515

Genes

NPHS2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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