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Protein substitute for children and adults with phenylketonuria (Cochrane Review)
Rutherford P, Poustie VJ

ABSTRACT

Background: Phenylketonuria is an inherited disease characterised by an absence or deficiency of the enzyme phenylalanine hydroxylase. The aim of treatment is to lower blood phenylalanine concentrations to prevent developmental delay. Current treatment is based . . .

Full article: The full article is available on Wiley InterScience at http://www.thecochranelibrary.com
Resources: WHO Reproductive Health Library, La Biblioteca Cochrane Plus, Renal Health Library, Malaria in Pregnancy Library
PubMed: Find related PubMed articles here [RutherfordP] [PoustieVJ] 
Google Scholar: Find related Google Scholar articles here [RutherfordP] [PoustieVJ]