Interaction of coding region mutations and the Gilbert-type promoter abnormality of the UGT1A1 gene causes moderate degrees of unconjugated hyperbilirubinaemia and may lead to neonatal kernicterus
Author:
Publisher
BMJ
Subject
Genetics (clinical),Genetics
Cited by 55 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Crigler Najjar syndrome type II with severe jaundice as a new subtype(?) : A rare case report;Clinics and Research in Hepatology and Gastroenterology;2024-08
2. A Rare Presentation of Indirect Hyperbilirubinemia: Coexistence of Multiple UGT1A1 Gene Variants;ACG Case Reports Journal;2024-07
3. Rare liver diseases in Egypt: Clinical and epidemiological characterization;Arab Journal of Gastroenterology;2024-05
4. Coexistence of mutations of Gilbert’s syndrome and Crigler-Najjar syndrome in an infant with unconjugated hyperbilirubinemia—a case report;Egyptian Pediatric Association Gazette;2023-10-09
5. Clinical and genetic definition of serum bilirubin levels for the diagnosis of Gilbert syndrome and hypobilirubinemia;Hepatology Communications;2023-09-22
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