Genetic Association of UGT1A1 Promoter Variants (c.-3279T>G and c.-3156G>A) with Neonatal Hyperbili-rubinemia in an Iranian Population

• Hoofdauteurs: Nasim Pouralizadeh (Auteur), Gholamali Mamouri (Auteur), Abbas Boskabadi (Auteur), Hassan Boskabadi (Auteur), Houshang Rafatpanah (Auteur), Ali Moradi (Auteur), Hassan Mehrad-Majd (Auteur)
• Formaat: Boek
• Gepubliceerd in: Mashhad University of Medical Sciences, 2021-04-01T00:00:00Z.
• Onderwerpen: article
• Online toegang: Connect to this object online.

Background: Several studies have reported that two promoter variants (c.-3279T>G and c.-3156G>A) in UDP-glucuronosyltransferase (UGT1A1) gene may contribute to neonatal hyperbilirubinemia. However, these variants have not been investigated in Iranian neonates. This cross-sectional study aimed...