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[Prolonged neonatal hyperbilirubinemia associated with a UGT1A1 gene mutation].

Anales de pediatria (Barcelona, Spain : 2003) - 1 Jun 2010

de la Fuente Juárez A, Viñallonga Sardà X, Capdevila Cogul E, Porta Ribera R

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Share to Glucuronosyltransferase
Share to Hyperbilirubinemia, Neonatal
Share to Infant, Newborn
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Identifiers

PMID: 20466608
DOI: 10.1016/j.anpedi.2010.03.002

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Prolonged Hyperbilirubinemia in a Neonate with a Novel Mutation in the UDP-glucuronosyltransferase 1A1 Gene.Semantic proximity Read ↗

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