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Article

Association analysis of the PHOX2B gene with Hirschsprung disease in the Han Chinese population of Southeastern China.

Journal of pediatric surgery - 1 Sept 2009

Liu Cui-Ping, Li Xin-Gang, Lou Jin-Tu, Xue Yun, Luo Chun-Fen, Zhou Xue-Wu, Chen Fei, Li Xiang, Li Meng, Li Ji-Cheng

Abstract excerpt

BACKGROUND: Hirschsprung disease (HSCR, OMIM 142623) is a complex congenital disorder characterized by intestinal obstructions caused by the absence of the intestinal ganglion cells of the nerve plexuses in variable lengths of the digestive tract. The PHOX2B gene is involved in neurogenesis and d...

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Identifiers

PMID: 19735829
DOI: 10.1016/j.jpedsurg.2008.12.009

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-19735829-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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Association analysis of the PHOX2B gene with Hirschsprung disease in the Han Chinese population of Southeastern China.PMID 19735829Read ↗

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