Cell encapsulation as a potential nondietary therapy for maternal phenylketonuria
Author:
Publisher
Elsevier BV
Subject
Obstetrics and Gynaecology
Reference43 articles.
1. Hyperphenylalaninemia: phenylalanine hydroxylase deficiency;Scriver,2001
2. Phenylketonuria and other phenylalanine hydroxylation mutants in man;Scriver;Annu Rev Genet,1980
3. The enzymatic conversion of phenylalanine to tyrosine;Udenfriend;J Biol Chem,1952
4. Phenylketonuria: screening and management consensus development conference statement;NIH,2000
5. Management of phenylketonuria for optimal outcome: a review of guidelines for phenylketonuria management and a report of surveys of parents, patients, and clinic directors;Wappner;Pediatrics,1999
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