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The role of UGT1A1 (c.-3279 T > G) gene polymorphisms in neonatal hyperbilirubinemia susceptibility
BACKGROUND: Neonatal hyperbilirubinemia (NNH) is a common disease in newborns. This research study aimed to assess the associations between uridine diphospho-glucuronate-glucuronosyltransferase 1A1 (UGT1A1, c.-3279 T > G) polymorphisms and NNH risk. METHODS: We searched PubMed, the Cochrane Libra...
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| Publicat a: | BMC Med Genet |
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| Autors principals: | , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BioMed Central
2020
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7648392/ https://ncbi.nlm.nih.gov/pubmed/33158427 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12881-020-01155-2 |
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