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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Kaydedildi:
Detaylı Bibliyografya
Yayımlandı:Biosci Rep
Asıl Yazarlar: Xie, Xiaoli, He, Qiuming, Huang, Lihua, Li, Le, Yao, Yuxiao, Xia, Huimin, Zhao, Jinglu, Zhong, Wei, Zhang, Yan
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Portland Press Ltd. 2019
Konular:
Research Articles
Online Erişim: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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