About
Site Map
Contact Us
Search
A service of the
U.S. National Library of Medicine®
Home
Conditions
Genes
Chromosomes
Handbook
Glossary
Resources
Genetic Conditions
>
phenylketonuria
>
References
These sources were used to develop the Genetics Home Reference
condition summary
on phenylketonuria.
Cederbaum S. Phenylketonuria: an update. Curr Opin Pediatr. 2002 Dec;14(6):702-6. Review.
PubMed citation
Clarke JT. The Maternal Phenylketonuria Project: a summary of progress and challenges for the future. Pediatrics. 2003 Dec;112(6 Pt 2):1584-7.
PubMed citation
de Baulny HO, Abadie V, Feillet F, de Parscau L. Management of phenylketonuria and hyperphenylalaninemia. J Nutr. 2007 Jun;137(6 Suppl 1):1561S-1563S; discussion 1573S-1575S.
PubMed citation
Gene Review: Phenylalanine Hydroxylase
Deficiency
Hanley WB. Adult phenylketonuria. Am J Med. 2004 Oct 15;117(8):590-5. Review.
PubMed citation
Scriver CR. The PAH gene, phenylketonuria, and a paradigm shift. Hum Mutat. 2007 Sep;28(9):831-45. Review.
PubMed citation
What you need to know about ... phenylketonuria. Nurs Times. 2003 Jul 29-Aug 4;99(30):26. Review.
PubMed citation
Reviewed: February 2012
Published: May 20, 2013