Publication | Closed Access
A mutation in bilirubin uridine 5′-diphosphate-glucuronosyltransferase isoform 1 causing Crigler-Najjar syndrome type II
101
Citations
19
References
1993
Year
Mendelian DisorderGenetic DisorderGeneticsPathogenesisInherited Metabolic DiseaseBiochemical GeneticsPathologyMolecular GeneticsDisease Gene IdentificationGenomicsMedicine
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