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A European Multicenter Study of Phenylalanine Hydroxylase Deficiency: Classification of 105 Mutations and a General System for Genotype-Based Prediction of Metabolic Phenotype

✍ Scribed by 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 Dianzani; Alberto Ponzone; Jean Rey; Flemming Güttler


Book ID
117852466
Publisher
American Society of Human Genetics
Year
1998
Tongue
English
Weight
124 KB
Volume
63
Category
Article
ISSN
0002-9297

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