Associations of SLC6A20 genetic polymorphisms with Hirschsprung’s disease in a Southern Chinese population

Hirschsprung’s disease (HSCR) is a neurodevelopmental disorder characterized by the absence of nerves in intestine with strong genetic components. SLC6A20 was found to be associated with HSCR in Korean population waiting for replication in an independent cohort. In the present study, ten single nucl...

Descripción completa

Detalles Bibliográficos
Autores principales: Xie, Xiaoli, He, Qiuming, Huang, Lihua, Li, Le, Yao, Yuxiao, Xia, Huimin, Zhao, Jinglu, Zhong, Wei, Zhang, Yan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2019
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6692567/
https://www.ncbi.nlm.nih.gov/pubmed/31358688
http://dx.doi.org/10.1042/BSR20182290

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6692567/
https://www.ncbi.nlm.nih.gov/pubmed/31358688
http://dx.doi.org/10.1042/BSR20182290

Ejemplares similares