权威例句
Hyperphenylalaninemia: Phenylalanine Hydroxylase DeficiencyTetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency ☆ ☆☆ ★Tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency, state of the artTetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency in Dutch neonates.Cloned human phenylalanine hydroxylase gene allows prenatal diagnosis and carrier detection of classical phenylketonuria.Molecular genetics of tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency.Molecular genetics of tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency †Mutational spectrum of phenylalanine hydroxylase deficiency in Sicily: implications for diagnosis of hyperphenylalaninemia in southe...Crystal structure of the catalytic domain of human phenylalanine hydroxylase reveals the structural basis for phenylketonuriaNucleotide sequence of a full-length complementary DNA clone and amino acid sequence of human phenylalanine hydroxylase.