Associations between UGT1A1 and SLCO1B1 polymorphisms and susceptibility to neonatal hyperbilirubinemia in Thai population

Hyperbilirubinemia is the main mechanism that causes neonatal jaundice, and genetics is one of the risk factors of hyperbilirubinemia. Therefore, this study aims to explore the correlation between two genes, UGT1A1 and SLCO1B1, and hyperbilirubinemia in Thai neonates. One hundred thirty seven neonat...

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Detalles Bibliográficos
Autores principales: Atasilp, Chalirmporn, Kanjanapipak, Janjira, Vichayaprasertkul, Jaratdao, Jinda, Pimonpan, Tiyasirichokchai, Rawiporn, Srisawasdi, Pornpen, Prempunpong, Chatchay, Chamnanphon, Monpat, Puangpetch, Apichaya, Vanwong, Natchaya, Klongthalay, Suwit, Jantararoungtong, Thawinee, Sukasem, Chonlaphat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9059389/
https://www.ncbi.nlm.nih.gov/pubmed/35501760
http://dx.doi.org/10.1186/s12887-022-03311-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9059389/
https://www.ncbi.nlm.nih.gov/pubmed/35501760
http://dx.doi.org/10.1186/s12887-022-03311-4

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