Structure of Tetrameric Human Phenylalanine Hydroxylase and Its Implications for Phenylketonuria
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference49 articles.
1. PAH Mutation Analysis Consortium Database: a database for disease- producing and other allelic variation at the human PAH locus
2. Molecular Basis of Phenotypic Heterogeneity in Phenylketonuria
3. Severity of mutation in the phenylalanine hydroxylase gene influences phenylalanine metabolism in phenylketonuria and hyperphenylalaninaemia heterozygotes
4. Structure and function of the aromatic amino acid hydroxylases
5. Crystal structure of the catalytic domain of human phenylalanine hydroxylase reveals the structural basis for phenylketonuria
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