Publication | Closed Access

Variations in genotype–phenotype correlations in phenylalanine hydroxylase deficiency in Chinese Han population

Genotype-phenotype AssociationGenetic DisorderMedicineGeneticsInherited Metabolic DiseaseGenotype–phenotype CorrelationsHuman PolymorphismPathologyMolecular GeneticsPhenylalanine Hydroxylase DeficiencyChinese Han Population