UGT1A1 Genetic Variations and a Haplotype Associated with Neonatal Hyperbilirubinemia in Indonesian Population

Neonatal hyperbilirubinemia (NH) is a common finding in newborn babies in Indonesia. Common and rare variants of UGT1A1 have been known to contribute to NH etiology. This study aims to identify UGT1A1 genetic variation and haplotype associated with NH in Indonesian population. DNA was isolated from...

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Pubblicato in:Biomed Res Int
Autori principali: Wisnumurti, Dewi A., Sribudiani, Yunia, Porsch, Robert M., Maskoen, Ani M., Abdulhamied, Lola I., Rahayuningsih, Sri E., Asni, Eni K., Sleutels, Frank, Kockx, Christel E. M., van Ijcken, Wilfred F. J., Sukadi, Abdurachman, Achmad, Tri H.
Natura: Artigo
Lingua:Inglês
Pubblicazione: Hindawi 2018
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Research Article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC5828093/
https://ncbi.nlm.nih.gov/pubmed/29607327
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2018/9425843
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