Phenylketonuria
Author:
Publisher
Wiley
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/9780470015902.a0006027
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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