Hepatology communications

· 1 paper in corpus
2023
doi:10.1097/hc9.0000000000000245 ·PMID:37738404

Background and aimsGilbert syndrome (GS) is genotypically predetermined by UGT1A1*28 homozygosity in Europeans and is phenotypically defined by hyperbilirubinemia using total bilirubin (TB) cutoff ≥1mg/dL (17 μmol/L). The prevalence of illn…