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

Abstract 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 sev...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Chalirmporn Atasilp, Janjira Kanjanapipak, Jaratdao Vichayaprasertkul, Pimonpan Jinda, Rawiporn Tiyasirichokchai, Pornpen Srisawasdi, Chatchay Prempunpong, Monpat Chamnanphon, Apichaya Puangpetch, Natchaya Vanwong, Suwit Klongthalay, Thawinee Jantararoungtong, Chonlaphat Sukasem
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: BMC 2022-05-01
Saila:BMC Pediatrics
Gaiak:
Genetic polymorphisms
UGT1A1
SLCO1B1
Hyperbilirubinemia
Neonates
Sarrera elektronikoa:https://doi.org/10.1186/s12887-022-03311-4
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