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Article

Low prevalence of NPHS2 mutations in African American children with steroid-resistant nephrotic syndrome.

Pediatric nephrology (Berlin, Germany) - 1 Sept 2008

Chernin Gil, Heeringa Saskia F, Gbadegesin Rasheed, Liu Jinhong, Hinkes Bernward G, Vlangos Christopher N, Vega-Warner Virginia, Hildebrandt Friedhelm

Abstract excerpt

In African American (AA) children, focal segmental glomerulosclerosis (FSGS) is the leading cause of nephrotic syndrome (NS). It has been shown that AA children suffer from FSGS and steroid-resistant nephrotic syndrome (SRNS) at a higher frequency and with a more severe renal outcome in compariso...

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Source

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Identifiers

PMID: 18543005
DOI: 10.1007/s00467-008-0861-7
PMCID: PMC5495478

Genes

NPHS2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-18543005-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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