Spectrum of PAH gene mutations and genotype-phenotype correlation in patients with phenylalanine hydroxylase deficiency from Turkey.
Müge ÇınarGonca Kilic YildirimSinem KocagilOğuz ÇilingirPublished in: Journal of pediatric endocrinology & metabolism : JPEM (2022)
genotype is the main factor that determines the phenotype of PKU. Establishing the relationship between the identified genetic mutations and phenotypic characteristics will provide very important data for each patient in terms of the specific management style.