G71R mutation of the UGT1A1 gene is not associated with neonatal hyperbilirubinemia in India

Also Consider

Synapse has enriched 4 closely related papers on similar clinical questions. Consider them for comparative context:

1. 1Neonatal hyperbilirubinemia and mutation of the bilirubin uridine diphosphate‐glucuronosyltransferase gene: a common missense mutation among Japanese, Koreans and Chinese1998 · 209 citations
2. 2Neonatal hyperbilirubinemia and G71R mutation of theUGT1A1gene in Turkish patients2010 · 15 citations
3. 3Genetic polymorphisms of bilirubin uridine diphosphate‐glucuronosyltransferase gene in Japanese patients with Crigler–Najjar syndrome or Gilbert's syndrome as well as in healthy Japanese subjects2004 · 97 citations
4. 4Gilbert’s syndrome: High frequency of the (TA)7TAA allele in India and its interaction with a novel CAT insertion in promoter of the gene for bilirubin UDP-glucuronosyltransferase 1 gene2006 · 61 citations