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Irrelevance of USF2 rs916145 polymorphism with the risk of biliary atresia susceptibility in Southern Chinese children
Author(s) -
Lei Chen,
Ming Fu,
Ledong Tan,
Jinglu Zhao,
Xiaogang Xu,
Yuzhen Lin,
Qian Zhong,
Ruisui Zhong,
Ruizhong Zhang,
Jixiao Zeng
Publication year - 2020
Publication title -
bioscience reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.938
H-Index - 77
eISSN - 1573-4935
pISSN - 0144-8463
DOI - 10.1042/bsr20193623
Subject(s) - odds ratio , genotype , gastroenterology , biliary atresia , confidence interval , etiology , polymorphism (computer science) , medicine , pathogenesis , genetics , biology , gene , transplantation , liver transplantation
Biliary atresia (BA) is a very rare neonatal disease, however, it has been the most common cause of obstructive jaundice in infancy. The complex pathogenesis of BA is not entirely clear and a lot of possible pathogenic mechanisms have been proposed to explain the etiology of BA, including genetic, inflammatory, environmental and developmental abnormalities. As a transcription factor, USF2 gene rs916145 polymorphism has been shown to be related to the risk of BA.

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