Title : A novel UGT1A1 gene mutation causing severe unconjugated hyperbilirubinemia: a case report.

Pub. Date : 2019 May 29

PMID : 31142299






1 Functional Relationships(s)
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Compound Name
Protein Name
Organism
1 CNs type II patients usually benefit from phenobarbital treatment that induces residual UGT1A1 activity. Phenobarbital UDP glucuronosyltransferase family 1 member A1 Homo sapiens