Association between ABHD1 and DOK6 polymorphisms and susceptibility to Hirschsprung disease in Southern Chinese children

Hirschsprung disease (HSCR) is an infrequent congenital intestinal dysplasia. The known genetic variations are unable to fully explain the pathogenesis of HSCR. The α/β‐hydratase domain 1 (ABHD1) interferes with the proliferation and migration of intestinal stem cells. Docking protein 6 (DOK6) is in...

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Detalles Bibliográficos
Autores principales: Lan, Chaoting, Wu, Yuxin, Wang, Ning, Luo, Yun, Zhao, Jinglu, Zheng, Yi, Zhang, Yan, Huang, Lihua, Zhu, Yun, Lu, Lifeng, Zhong, Wei, Zeng, Jixiao, Xia, Huimin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8505836/
https://www.ncbi.nlm.nih.gov/pubmed/34545688
http://dx.doi.org/10.1111/jcmm.16905

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8505836/
https://www.ncbi.nlm.nih.gov/pubmed/34545688
http://dx.doi.org/10.1111/jcmm.16905

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