Phenylketonuria

Author:

Güttler Flemming,Guldberg Per

Publisher

Wiley

Reference23 articles.

1. Missense Mutations in the N-Terminal Domain of Human Phenylalanine Hydroxylase Interfere with Binding of Regulatory Phenylalanine

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

3. Hyperphenylalaninemia: diagnosis and classification of the various types of phenylalanine hydroxylase deficiency;Güttler F;Acta Paediatrica Scandinavica,1980

4. Phenylketonuria: 50 Years since Felling's Discovery and still Expanding our Clinical and Biochemical Knowledge

5. Mutation genotype of mentally retarded patients with phenylketonuria;Güttler F;Develop‐mental Brain Dysfunction,1993

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