Phenylalanine hydroxylase deficiency caused by a single base substitution in an exon of the human phenylalanine hydroxylase gene

Uta Lichter-Konecki, David S. Konecki, Anthony G. DiLella, Kelly Brayton, Joshua Marvit, Tina M. Hahn, Fritz K. Trefz, Savio L. C. Woo
Biochemistry, 1988, 27 (8), pp 2881–2885
DOI: 10.1021/bi00408a032
Publication Date: April 1988
ACS Legacy Archive

Note: In lieu of an abstract, this is the article's first page.

View: Hi-Res PDF

Tools

SciFinder Links

SciFinder subscribers: Click to sign in | Not a SciFinder subscriber? Learn more at www.cas.org

History

  • Published In Issue April, 1988

Recommend & Share