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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Vydáno v:Biomed Res Int
Hlavní autoři: 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.
Médium: Artigo
Jazyk:Inglês
Vydáno: Hindawi 2018
Témata:
Research Article
On-line přístup: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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