Cargando…
Susceptibility of ECE1 polymorphisms to Hirschsprung's disease in southern Chinese children
BACKGROUND: Hirschsprung's disease (HSCR) is currently considered to be a congenital gastrointestinal malformation caused mainly by genetic factors. Endothelin Converting Enzyme-1 (ECE1) has been reported to be associated with HSCR. However, the relationship between ECE1 single nucleotide polym...
Autores principales: | Lan, Chaoting, Liu, Yanqing, Wu, Xiao, Wang, Bingtong, Xin, Songqing, He, Qiuming, Zhong, Wei, Liu, Zipeng |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9813666/ https://www.ncbi.nlm.nih.gov/pubmed/36619519 http://dx.doi.org/10.3389/fped.2022.1056938 |
Ejemplares similares
-
Susceptibility of PCSK2 Polymorphism to Hirschsprung Disease in Southern Chinese Children
por: Wang, Bingtong, et al.
Publicado: (2023) -
Plasma single-stranded DNA autoantibodies in the diagnosis of Hirschsprung’s disease
por: Wang, Bingtong, et al.
Publicado: (2022) -
Association between ABHD1 and DOK6 polymorphisms and susceptibility to Hirschsprung disease in Southern Chinese children
por: Lan, Chaoting, et al.
Publicado: (2021) -
Association between IKBKAP polymorphisms and Hirschsprung’s disease susceptibility in Chinese children
por: Wang, Ning, et al.
Publicado: (2022) -
Associations of CYP2B6 genetic polymorphisms with Hirschsprung’s disease in a southern Chinese population
por: Liu, Yanqing, et al.
Publicado: (2021)