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

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

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...

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Bibliographic Details
Main Authors: Nasim Pouralizadeh, Gholamali Mamouri, Abbas Boskabadi, Hassan Boskabadi, Houshang Rafatpanah, Ali Moradi, Hassan Mehrad-Majd
Format: Article
Language:English
Published: Mashhad University of Medical Sciences 2021-04-01
Series:Iranian Journal of Neonatology
Subjects:
hyperbilirubinemia
kernicterus
polymorphism
ugt1a1
Online Access:https://ijn.mums.ac.ir/article_17519_434c45c56cc4487602c8d7784ff3b244.pdf

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