Publication | Closed Access

Frequent co-occurrence of the TATA box mutation associated with Gilbert’s syndrome (UGT1A1*28) with other polymorphisms of the UDP-glucuronosyltransferase-1 locus (UGT1A6*2 and UGT1A7*3) in Caucasians and Egyptians

Mendelian DisorderGenetic DisorderMedicineGeneticsInherited Metabolic DiseaseGenetic EpidemiologyOther PolymorphismsPathologyHuman PolymorphismMolecular GeneticsMedical GeneticsDisease Gene IdentificationPublic HealthTata Box MutationGilbert ’Monogenic Disorders