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...

Descripción completa

Detalles Bibliográficos
Autores principales: Li, Zijin, Song, Li, Hao, Lihong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7648392/
https://www.ncbi.nlm.nih.gov/pubmed/33158427
http://dx.doi.org/10.1186/s12881-020-01155-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7648392/
https://www.ncbi.nlm.nih.gov/pubmed/33158427
http://dx.doi.org/10.1186/s12881-020-01155-2

Ejemplares similares