A novel deletion mutation (c.749 del C) in the UGT1A1 gene as a cause of Crigler-Najjar syndrome type 1: A case report
Article in Gene Reports (June 2021)
The most recent citing publications are shown below. View all 6 publications that cite this research output on Dimensions.
Analysis of mutation site characteristics of Gilbert syndrome and Crigler--Najjar syndrome in relation to uridine diphosphate glucuronosyltransferase A1 gene
Article in Chinese Journal of Hepatology (May 2020)
A novel deletion with two pathogenic variants of UGT1A1 causing Crigler-Najjar syndrome in two unrelated Chinese
Article in Clinical Biochemistry (June 2019)