Publication | Closed Access

Phenylalanine hydroxylase deficiency in the Slovak population: Genotype–phenotype correlations and genotype-based predictions of BH4-responsiveness

BiochemistryGenetic DisorderMedicineGeneticsInherited Metabolic DiseaseGenetic EpidemiologyGenotype–phenotype CorrelationsMedical GeneticsPhenylalanine Hydroxylase DeficiencySlovak Population