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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Detalhes bibliográficos
Publicado no:Biomed Res Int
Main Authors: 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.
Formato: Artigo
Idioma:Inglês
Publicado em: Hindawi 2018
Assuntos:
Research Article
Acesso em linha: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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