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Article

WT1 gene mutations in Chinese children with early onset nephrotic syndrome.

Pediatric research - 1 Aug 2010

Li Jianguo, Ding Jie, Zhao Dan, Yu Zihua, Fan Qingfeng, Chen Yan, Zhang Hongwen, Zhong Xuhui, Huang Jianping, Yao Yong, Xiao Huijie

Abstract excerpt

In Chinese children with steroid-resistant nephrotic syndrome (SRNS), it was reported that NPHS2 mutation was detected in 4.3%, which was lower than that in Caucasians (10-30%). However, there were no data on WT1 mutation in nephrotic syndrome (NS), especially in early-onset NS of Chinese children. Thus, a study, which enrolled 36 Chinese children with early-onset (before 3 y old) NS and steroid resistance if...

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Source

Identifiers

PMID: 20442690
DOI: 10.1203/PDR.0b013e3181e4c9e3

Genes

NPHS2

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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