Publication | Open Access
A New Type of Defect in the Gene for Bilirubin Uridine 5 '-Diphosphate-Glucuronosyltransferase in a Patient with Crigler-Najjar Syndrome Type I
74
Citations
20
References
1994
Year
Mendelian DisorderNew TypeGenetic DisorderGeneticsPathogenesisInherited Metabolic DiseaseIga GlomerulonephritisPathologyMolecular GeneticsCrigler-najjar Syndrome TypeDisease Gene IdentificationMedicineBilirubin Uridine 5
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