Profiling of UGT1A1(*)6, UGT1A1(*)60, UGT1A1(*)93, and UGT1A1(*)28 Polymorphisms in Indonesian Neonates With Hyperbilirubinemia Using Multiplex PCR Sequencing

Background: Single nucleotide polymorphism (SNP) variants of the uridine diphosphate glucuronosyltransferase 1A1 (UGT1A1) gene have been studied as an important factor in neonatal hyperbilirubinemia (jaundice) severity. Specific ethnicities, including Asians, have certain SNPs that appear more frequ...

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Bibliografiska uppgifter
I publikationen:Front Pediatr
Huvudupphovsmän: Amandito, Radhian, Rohsiswatmo, Rinawati, Carolina, Erica, Maulida, Rizka, Kresnawati, Windhi, Malik, Amarila
Materialtyp: Artigo
Språk:Inglês
Publicerad: Frontiers Media S.A. 2019
Ämnen:
Pediatrics
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC6693044/
https://ncbi.nlm.nih.gov/pubmed/31440488
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fped.2019.00328
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