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Article

Absence of PAX2 gene mutations in patients with primary familial vesicoureteric reflux.

Journal of medical genetics - 1 Apr 1998

Choi K L, McNoe L A, French M C, Guilford P J, Eccles M R

Abstract excerpt

Vesicoureteric reflux (VUR) is a common childhood condition characterised by regurgitation of urine from the bladder to the kidney. It is the commonest cause of end stage renal failure in children and an important cause in adults. Primary VUR is often familial, suggesting that genetic factors pla...

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Identifiers

PMID: 9598733
DOI: 10.1136/jmg.35.4.338
PMCID: PMC1051287

Genes

PAX2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-9598733-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

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

Related research

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Absence of PAX2 gene mutations in patients with primary familial vesicoureteric reflux.PMID 9598733Read ↗

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ROBO2 gene variants are associated with familial vesicoureteral reflux.Semantic proximity Read ↗

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ROBO2 gene variants in children with primary nonsyndromic vesicoureteral reflux with or without renal hypoplasia/dysplasia.Semantic proximity Read ↗

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