Phenylalanine ammonia lyase (PAL): From discovery to enzyme substitution therapy for phenylketonuria
Author:
Publisher
Elsevier BV
Subject
Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism
Reference71 articles.
1. Phenylketonuria: epitome of human biochemical genetics;Scriver;N. Engl. J. Med.,1980
2. 77: Hyperphenylalaninemia: phenylalanine hydroxylase deficiency;Donlon,2014
3. Phenylketonuria;Blau;Lancet,2010
4. Phenylalanine hydroxylase deficiency: diagnosis and management guideline;Vockley;Genet. Med.,2014
5. Key European guidelines for the diagnosis and management of patients with phenylketonuria;van Spronsen;Lancet Diabetes Endocrinol.,2017
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