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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Detalhes bibliográficos
Main Authors: Hanchard, Neil A, Skierka, Jennifer, Weaver, Amy, Karon, Brad S, Matern, Dietrich, Cook, Walter, O'Kane, Dennis J
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2011
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3107779/
https://ncbi.nlm.nih.gov/pubmed/21513526
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2350-12-57
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