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Identification of Defect in the Genes for Bilirubin UDP-Glucuronosyltransferase in a Patient with Crigler-Najjar Syndrome Type II

Mendelian DisorderGenetic DisorderGeneticsPathogenesisInherited Metabolic DiseaseHematologyPathologyBilirubin Udp-glucuronosyltransferaseMolecular GeneticsDisease Gene IdentificationMedicineInborn Error Of ImmunityClinical Genetics