Publication | Open Access

Genotype–phenotype correlation in primary hyperoxaluria type 1: the p.Gly170Arg AGXT mutation is associated with a better outcome

Allelic VariantPrimary HyperoxaluriaGenetic DisorderMedicineGeneticsInherited Metabolic DiseaseGenetic EpidemiologyGenotype–phenotype CorrelationPathologyP.gly170arg Agxt MutationHuman PolymorphismMolecular DiagnosticsClinical Genetics