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Do Gene Polymorphisms Play a Role in Newborn Hyperbilirubinemia?
- Source :
- Balkan Journal of Medical Genetics, Vol 26, Iss 2, Pp 51-58 (2024)
- Publication Year :
- 2024
- Publisher :
- Sciendo, 2024.
-
Abstract
- Polymorphisms of the uridine-diphospho-glucuronosyltransferase 1A1 (UGT1A1) gene, hepatic solute carrier organic anion transporter 1B1/B3 (SLCO1B1/3) gene, and glutathione S-transferase (GST) gene have been associated with significant hyperbilirubinemia in some populations. This study aims to determine whether the variation of UGT1A1, SLCO1B1/3 and GST genes play an important role in neonatal hyperbilirubinemia in Turkish newborn infants.
Details
- Language :
- English
- ISSN :
- 21995761
- Volume :
- 26
- Issue :
- 2
- Database :
- Directory of Open Access Journals
- Journal :
- Balkan Journal of Medical Genetics
- Publication Type :
- Academic Journal
- Accession number :
- edsdoj.f0a167a8bd11475581a4bd49a09a51d2
- Document Type :
- article
- Full Text :
- https://doi.org/10.2478/bjmg-2023-0021