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Correlation analysis of IL-11 polymorphisms and Hirschsprung disease subtype susceptibility in Southern Chinese Children

BACKGROUND: Hirschsprung disease (HSCR) is a hereditary defect, which is characterized by the absence of enteric ganglia and is frequently concurrent with Hirschsprung-associated enterocolitis (HAEC). However, the pathogenesis for HSCR is complicated and remains unclear. Recent studies have shown th...

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Detalles Bibliográficos
Autores principales: Zhang, Hong, Zhao, Jing-Lu, Zheng, Yi, Xie, Xiao-Li, Huang, Li-Hua, Li, Le, Zhu, Yun, Lu, Li-Feng, Hu, Tu-Qun, Zhong, Wei, He, Qiu-Ming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7814452/
https://www.ncbi.nlm.nih.gov/pubmed/33468134
http://dx.doi.org/10.1186/s12920-020-00867-x