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Article

A genome search for primary vesicoureteral reflux shows further evidence for genetic heterogeneity.

Pediatric nephrology (Berlin, Germany) - 1 Apr 2008

Conte Maria Luisa, Bertoli-Avella Aida M, de Graaf Bianca M, Punzo Francesca, Lama Giuliana, La Manna Angela, Grassia Carolina, Rambaldi Pier Francesco, Oostra Ben A, Perrotta Silverio

Abstract excerpt

Vesicoureteral reflux (VUR) is the most common disease of the urinary tract in children. In order to identify gene(s) involved in this complex disorder, we performed a genome-wide search in a selected sample of 31 patients with primary VUR from eight families originating from southern Italy. Sixteen additional families with 41 patients were included in a second stage. Nonparametric, affected-only linkage analysis...

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Identifiers

PMID: 18197425
DOI: 10.1007/s00467-007-0675-z
PMCID: PMC2259258

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NPL

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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A genome search for primary vesicoureteral reflux shows further evidence for genetic heterogeneity.PMID 18197425Read ↗

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