A European Multicenter Study of Phenylalanine Hydroxylase Deficiency: Classification of 105 Mutations and a General System for Genotype-Based Prediction of Metabolic Phenotype
Per Guldberg, Françoise Rey, Johannes Zschocke, Valentino Romano, Baudouin François, Luc Michiels, Kurt Ullrich, Georg F. Hoffmann, Peter Burgard, Hildgund Schmidt, Concetta Meli, Enrica Riva, Irma DiVolume:
63
Year:
1998
Language:
english
DOI:
10.1086/301920
File:
PDF, 124 KB
english, 1998