Publication | Open Access

Genetic and biochemical study of dual hereditary jaundice: Dubin–Johnson and Gilbert’s syndromes. Haplotyping and founder effect of deletion in ABCC2

Genetic DisorderGeneticsInherited Metabolic DiseaseHematologyPathologyMolecular GeneticsMedical GeneticsDisease Gene IdentificationBiochemical StudyDual Hereditary JaundiceFounder EffectMedicineGenetic MedicineGenetic BasisClinical Genetics