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Article

A novel mutation of NPHS2 identified in a Chinese family.

Pediatric nephrology (Berlin, Germany) - 1 Nov 2004

Yu Zihua, Ding Jie, Guan Na, Shi Yan, Zhang Jingjing, Huang Jianping, Yao Yong, Yang Jiyun

Abstract excerpt

Since the identification of the NPHS2 gene,which encodes podocin, several groups from European, Middle Eastern, and North American countries have reported NPHS2 mutations in families with steroid-resistant nephrotic syndrome (SRNS) or focal segmental glomerulo sclerosis (FSGS). Families with SRNS...

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Source

Identifiers

PMID: 15322893
DOI: 10.1007/s00467-004-1585-y

Genes

NPHS2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-15322893-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 1 Sept 2026.

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