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Article

Significant Association of rs2147555 Genetic Polymorphism in the EDNRB Gene with Hirschsprung Disease in Southern Chinese Children.

BioMed research international - 1 Jan 2020

Zheng Yi, Lan ChaoTing, Wang Ning, Xu Xiaogang, Hu Tuqun, Wu Qi, Xie Xiaoli, Wang Zhe, Zhang Yan, Li Cong

Abstract excerpt

Hirschsprung disease (HSCR) is a human birth defect at the clinical setting, usually characterized by an absent enteric nervous system (ENS) from the distal bowel. The majority of HSCR cases represent a complex disorder resulting from the interaction of multiple genetic and environmental factors. Genetic events have been described to be involved in the abnormal development of the enteric nervous system. Although...

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Identifiers

PMID: 33178831
DOI: 10.1155/2020/5956412
PMCID: PMC7648675

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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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