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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Publicat a:Biomed Res Int
Autors principals: Zheng, Yi, Lan, ChaoTing, Wang, Ning, Xu, Xiaogang, Hu, Tuqun, Wu, Qi, Xie, Xiaoli, Wang, Zhe, Zhang, Yan, Li, Cong
Format: Artigo
Idioma:Inglês
Publicat: Hindawi 2020
Matèries:
Research Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC7648675/
https://ncbi.nlm.nih.gov/pubmed/33178831
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2020/5956412
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