Neonatal hyperbilirubinemia and G71R mutation of the UGT1A1 gene in Turkish patients

No abstract is available for this paper.

• Publication year

  2011

• Venue

  Journal of Maternal-Fetal & Neonatal Medicine

• Publication date

  2011-01-13

• Fields of study

  Medicine

• Identifiers
  DOI 10.3109/14767058.2010.490889PMID 20528217
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Neonatal jaundice and liver disease

  2011cited by this paper
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  2002influential reference
• Gly71Arg mutation of the bilirubin UDP-glucuronosyltransferase 1A1 gene is associated with neonatal hyperbilirubinemia in the Japanese population.

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  2002influential reference
• Prolonged Unconjugated Hyperbilirubinemia Associated With Breast Milk and Mutations of the Bilirubin Uridine Diphosphate- Glucuronosyltransferase Gene

  2000cited by this paper
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• Cloning of two human liver bilirubin UDP-glucuronosyltransferase cDNAs with expression in COS-1 cells.

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