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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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Detalles Bibliográficos
Autores principales:	Amandito, Radhian, Rohsiswatmo, Rinawati, Carolina, Erica, Maulida, Rizka, Kresnawati, Windhi, Malik, Amarila
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2019
Materias:	Pediatrics
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6693044/ https://www.ncbi.nlm.nih.gov/pubmed/31440488 http://dx.doi.org/10.3389/fped.2019.00328

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