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Article

Genetics of human congenital urinary bladder disease.

Pediatric nephrology (Berlin, Germany) - 1 Mar 2014

Woolf Adrian S, Stuart Helen M, Newman William G

Abstract excerpt

Lower urinary tract and/or kidney malformations are collectively the most common cause of end-stage renal disease in children, and they are also likely to account for a major subset of young adults requiring renal replacement therapy. Advances have been made regarding the discovery of the genetic causes of human kidney malformations. Indeed, testing for mutations of key nephrogenesis genes is now feasible for...

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Identifiers

PMID: 23584850
DOI: 10.1007/s00467-013-2472-1

Genes

ACTA2
CHRM3
HPSE2

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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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