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Article

Polymorphisms and expression of the WNT8A gene in Hirschsprung's disease.

International journal of molecular medicine - 1 Sept 2013

Gao Hong, Chen Dong, Liu Xiaomei, Wu Mei, Mi Jie, Wang Weilin

Abstract excerpt

Hirschsprung's disease (HSCR) is a congenital disorder characterized by an absence of intrinsic ganglion cells in the nerves forming the plexus of the lower intestine. The WNT signaling pathway is considered to play an important role in embryonic development. In the present study, we analyzed 2 polymorphisms of the WNT8A gene (rs78301778 and rs6596422) to determine their association with the risk and development...

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Identifiers

PMID: 23836442
DOI: 10.3892/ijmm.2013.1433

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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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