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Article

NPHS2 (Podocin) mutations in nephrotic syndrome. Clinical spectrum and fine mechanisms.

Pediatric research - 1 May 2005

Caridi Gianluca, Perfumo Francesco, Ghiggeri Gian Marco

Abstract excerpt

Nephrotic syndrome (NS) is the most frequent cause of proteinuria in children and is emerging as a leading cause of uremia. Molecular studies in families with recessive NS have led to the discovery of specialized molecules endowed in podocytes that play a role in proteinuria. This review focalize...

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Source

Identifiers

PMID: 15817495
DOI: 10.1203/01.PDR.0000160446.01907.B1

Genes

NPHS2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-15817495-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

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

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NPHS2 (Podocin) mutations in nephrotic syndrome. Clinical spectrum and fine mechanisms.PMID 15817495Read ↗

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Clinical features and long-term outcome of nephrotic syndrome associated with heterozygous NPHS1 and NPHS2 mutations.Semantic proximity Read ↗

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