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Association between IKBKAP polymorphisms and Hirschsprung’s disease susceptibility in Chinese children

BACKGROUND: Hirschsprung’s disease (HSCR) is a rare congenital disease in which enteric nervous system (ENS) in the distal intestine is absent. HSCR is a disease involving genetic factors and environmental factors. Despite a series of genes have been revealed to contribute to HSCR, many HSCR associa...

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Detalles Bibliográficos
Autores principales:	Wang, Ning, Xi, Jiaojiao, Lan, Chaoting, Wu, Yuxin, Zhu, Yun, Zuo, Xiaoyu, Zhang, Yan
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	AME Publishing Company 2022
Materias:	Original Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9253937/ https://www.ncbi.nlm.nih.gov/pubmed/35800263 http://dx.doi.org/10.21037/tp-21-550

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