A European multi-center study of phenylalanine hydroxylase deficiency: classification of 105 mutations and a general system for genotype-based prediction of metabolic phenotype

Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/5848

Title:	A European multi-center study of phenylalanine hydroxylase deficiency: classification of 105 mutations and a general system for genotype-based prediction of metabolic phenotype
Authors:	Guldberg, P. Rey, F. Zschocke, J. Romano, V. FRANCOIS, Baudouin MICHIELS, Luc Ullrich, K. Hoffmann, G. Burgard, P. Schmidt, H. Meli, C. Riva, E. Dianzani, I. Ponzone, A. Rey, J. Güttler, F.
Issue Date:	1998
Source:	The American journal of human genetics, 63. p. 71-79
Document URI:	http://hdl.handle.net/1942/5848
ISI #:	000074761000012
Type:	Journal Contribution
Validations:	ecoom 1999
Appears in Collections:	Research publications

Check