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Citation: A. Kadakol et al., Interaction of coding region mutations and the Gilbert-type promoter abnormality of the UGT1A1 gene causes moderate degrees of unconjugated hyperbilirubinaemia and may lead to neonatal kernicterus, J MED GENET, 38(4), 2001, pp. 244-249

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Authors: Kadakol, A Ghosh, SS Sappal, BS Sharma, G Chowdhury, JR Chowdhury, NR

Citation: A. Kadakol et al., Genetic lesions of bilirubin uridine-diphosphoglucuronate glucuronosyltransferase (UGT1A1) causing Crigler-Najjar and Gilbert syndromes: Correlation of genotype to phenotype, HUM MUTAT, 16(4), 2000, pp. 297-306