Associated Papers
Genetic testing of UGT1A1 in the diagnosis of Gilbert syndrome: The discovery of seven novel variants in the Chinese population.
Gu L et al.
Molecular Genetics & Genomic Medicine, 2022
Red blood cell PK deficiency: An update of PK-LR gene mutation database.
Canu G et al.
Blood Cells, Molecules & Diseases, 2016
[From gene to disease; unconjugated hyperbilirubinemia: Gilbert's syndrome and Crigler-Najjar types I and II].
Drenth JP et al.
Nederlands Tijdschrift Voor Geneeskunde, 2002
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