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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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2018
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5828093/
https://www.ncbi.nlm.nih.gov/pubmed/29607327
http://dx.doi.org/10.1155/2018/9425843

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5828093/
https://www.ncbi.nlm.nih.gov/pubmed/29607327
http://dx.doi.org/10.1155/2018/9425843

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