1. Hyperphenylalaninemia: phenylalanine hydroxylase deficiency;Scriver,2001
2. The enzymatic conversion of phenylalanine to tyrosine;Udenfriend;J. Biol. Chem.,1952
3. Intellectual development in 12-year-old children treated for phenylketonuria;Azen;Am. J. Dis. Child.,1991
4. Gene therapy for phenylketonuria: phenotypic correction in a genetically deficient mouse model by adenovirus-mediated hepatic gene therapy;Fang;Gene Ther.,1994
5. Principles of hepatocyte repopulation;Laconi;Semin. Cell Dev. Biol.,2002