Refine Your Results

Click below to filter your search results

"Birth Defects"Undo
"Nutrition - Exercise"Undo
"Committee Opinion"Undo
Return to List
Results 1–1 of 1
Title Date
1.

Maternal Phenylketonuria

Number 449

(Replaces No. 230, January 2000)

ABSTRACT: Phenylketonuria (PKU) is an autosomal recessive disorder of phenylalanine (Phe) metabolism characterized by a deficiency of the hepatic enzyme, phenylalanine hydroxylase, an enzyme responsi...

December 2009

PDF Format