UGT1A1 sequence variants and bilirubin levels in early postnatal life: a quantitative approach

BACKGROUND: Fundamental to definitively identifying neonates at risk of developing significant hyperbilirubinemia is a better understanding of the genetic factors associated with early bilirubin rise. Previous genetic studies have focused on the UGT1A1 gene, associating common variation in the codin...

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Detalles Bibliográficos
Autores principales: Hanchard, Neil A, Skierka, Jennifer, Weaver, Amy, Karon, Brad S, Matern, Dietrich, Cook, Walter, O'Kane, Dennis J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3107779/
https://www.ncbi.nlm.nih.gov/pubmed/21513526
http://dx.doi.org/10.1186/1471-2350-12-57

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3107779/
https://www.ncbi.nlm.nih.gov/pubmed/21513526
http://dx.doi.org/10.1186/1471-2350-12-57

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