Publication | Closed Access

Contribution of two missense mutations (G71R and Y486D) of the bilirubin UDP glycosyltransferase (UGT1A1) gene to phenotypes of Gilbert's syndrome and Crigler–Najjar syndrome type II

Transcriptional RegulationMissense MutationsMendelian DisorderBilirubin Udp GlycosyltransferaseGenetic DisorderGeneticsInherited Metabolic DiseasePathologyMolecular GeneticsDisease Gene IdentificationGenomicsGene ExpressionMedicineType Ii