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Article

Genetic polymorphism of NPHS1 modifies the clinical manifestations of Ig A nephropathy.

Laboratory investigation; a journal of technical methods and pathology - 1 Aug 2003

Narita Ichiei, Goto Shin, Saito Noriko, Song Jin, Kondo Daisuke, Omori Kentaro, Kawachi Hiroshi, Shimizu Fujio, Sakatsume Minoru, Ueno Mitsuhiro, Gejyo Fumitake

Abstract excerpt

Nephrin, the molecule responsible for congenital nephrotic syndrome of Finnish type, is crucial in maintaining the glomerular filtration barrier. Recently, its complete gene structure and common gene polymorphisms in its exons have been reported, although the functional and clinical significance...

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Source

Identifiers

PMID: 12920248
DOI: 10.1097/01.lab.0000080600.49276.31

Genes

NPHS1

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-12920248-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

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

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Genetic polymorphism of NPHS1 modifies the clinical manifestations of Ig A nephropathy.PMID 12920248Read ↗

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