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

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. Ge...

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Detalles Bibliográficos
Autores principales:	Zheng, Yi, Lan, ChaoTing, Wang, Ning, Xu, Xiaogang, Hu, Tuqun, Wu, Qi, Xie, Xiaoli, Wang, Zhe, Zhang, Yan, Li, Cong
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Hindawi 2020
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7648675/ https://www.ncbi.nlm.nih.gov/pubmed/33178831 http://dx.doi.org/10.1155/2020/5956412

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