Article
Associations between common genetic variants in microRNAs and Hirschsprung disease susceptibility in Southern Chinese children.
The journal of gene medicine - 1 Feb 2021
Wu Qi, Zhao Jinglu, Zheng Yi, Xie Xiaoli, He Qiuming, Zhu Yun, Wang Ning, Huang Lihua, Lu Lifeng, Hu Tuqun, Zeng Jixiao, Xia Huimin, Zhang Yan, Zhong Wei
Abstract excerpt
INTRODUCTION: Hirschsprung disease (HSCR), characterized by the defective migration of enteric neural crest cells, is a severe congenital tract disease in infants. Its etiology is not clear at present, although a genetic component plays an important role in its etiology. Many studies focused on the polymorphisms of microRNA (miRNA) in several disease progressions have been reported, including HSCR. However, the...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
