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...

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Bibliographic Details
Published in:Biosci Rep
Main Authors: Xie, Xiaoli, He, Qiuming, Huang, Lihua, Li, Le, Yao, Yuxiao, Xia, Huimin, Zhao, Jinglu, Zhong, Wei, Zhang, Yan
Format: Artigo
Language:Inglês
Published: Portland Press Ltd. 2019
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Research Articles
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC6692567/
https://ncbi.nlm.nih.gov/pubmed/31358688
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1042/BSR20182290
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