Erratum: A European Multicenter Study of Phenylalanine Hydroxylase Deficiency: Classification of 105 Mutations and a General System for Genotype-Based Prediction of Metabolic Phenotype (The American Journal of Human Genetics (1998) 63(1) (71–79) (S0002929707607605) (10.1086/301920));A European multicenter study of phenylalanine hydroxylase deficiency: Classification of 105 mutations and a general system for genotype-based prediction of metabolic phenotype

American Journal of Human Genetics

Volumn 63, Issue 1, 1998, Pages 71-79

  Guldberg, Per ^a   Rey, Françoise ^b   Zschocke, Johannes ^c   Romano, Valentino ^d   François, Baudouin ^e   Michiels, Luc ^e   Ullrich, Kurt ^f   Hoffmann, Georg F ^c   Burgard, Peter ^g   Schmidt, Hildgund ^g   Meli, Concetta ^h   Riva, Enrica ⁱ   Dianzani, Irma ^j   Ponzone, Alberto ^j   Rey, Jean ^b   Güttler, Flemming ^a  

^a JOHN F KENNEDY INSTITUTE   (Denmark)

^b HÔPITAL NECKER ENFANTS MALADES   (France)

^c University Children's Hospital   (Germany)

^d Laboratorio di Genetica Molecolare   (Italy)

^e HASSELT UNIVERSITY   (Belgium)

^f UNIVERSITY MEDICAL CENTER HAMBURG EPPENDORF   (Germany)

^g UNIVERSITY OF HEIDELBERG   (Germany)

^h UNIVERSITY OF CATANIA   (Italy)

ⁱ UNIVERSITY OF MILAN   (Italy)

^j UNIVERSITY OF TURIN   (Italy)

more..

Author keywords

[No Author keywords available]

Indexed keywords

PHENYLALANINE 4 MONOOXYGENASE;

ARTICLE; CLINICAL TRIAL; DISEASE CLASSIFICATION; ENZYME DEFICIENCY; GENOTYPE; HUMAN; HUMAN CELL; HUMAN TISSUE; MAJOR CLINICAL STUDY; MULTICENTER STUDY; PHENOTYPE; PHENYLKETONURIA; PREDICTION; PRIORITY JOURNAL;

EID: 0032231461     PISSN: 00029297     EISSN: 15376605     Source Type: Journal    
DOI: 10.1016/S0002-9297(07)61825-4     Document Type: Erratum

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