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Novel mutation in the GRHPR gene in a Chinese patient with primary hyperoxaluria type 2 requiring renal transplantation from a living related donor

Chinese PatientUrologyMendelian DisorderKidney TransplantPrimary HyperoxaluriaGenetic DisorderGeneticsInherited Metabolic DiseaseHuman PolymorphismPathologyGrhpr GeneDisease Gene IdentificationMedicineNephrology