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Crigler-Najjar syndrome type II in a Chinese boy resulting from three mutations in the bilirubin uridine 5′-diphosphate-glucuronosyltransferase (UGT1A1) gene and a family genetic analysis

Crossref DOI link: https://doi.org/10.1186/1471-2431-14-267

Published Online: 2014-10-15

Published Print: 2014-12

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