Correlation of UGT1A1 genotypes with newborn hyperbilirubinemia using newborn genetic screening
BackgroundThis study evaluated whether uridine diphosphate glucuronosyltransferase 1A1 (UGT1A1) variants identified through newborn genetic screening are associated with the development of clinically significant neonatal hyperbilirubinemia.MethodsNext-generation sequencing (NGS) was performed in 1,0...
-д хадгалсан:
| Үндсэн зохиолчид: | , , , , |
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| Формат: | Artigo |
| Хэл сонгох: | Inglês |
| Хэвлэсэн: |
Frontiers Media S.A.
2026-07-01
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| Цуврал: | Frontiers in Pediatrics |
| Нөхцлүүд: | |
| Онлайн хандалт: | https://www.frontiersin.org/articles/10.3389/fped.2026.1737797/full |
| Шошгууд: |
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