STUDIES ON PHENYLKETONURIA. I. RESTRICTED PHENYLALANINE INTAKE IN PHENYLKETONURIA

Marvin D. Armstrong; Frank H. Tyler

doi:10.1172/JCI103105

^{Laboratory for the Study of Hereditary and Metabolic Disorders, and the Department of Biochemistry, University of Utah College of Medicine, Salt Lake City, Utah}

^{Laboratory for the Study of Hereditary and Metabolic Disorders, and the Department of Medicine, University of Utah College of Medicine, Salt Lake City, Utah}

This work was supported by research grants from the National Institutes of Health, U. S. Public Health Service.

Find articles by Armstrong, M. in: PubMed | Google Scholar

^{Laboratory for the Study of Hereditary and Metabolic Disorders, and the Department of Biochemistry, University of Utah College of Medicine, Salt Lake City, Utah}

^{Laboratory for the Study of Hereditary and Metabolic Disorders, and the Department of Medicine, University of Utah College of Medicine, Salt Lake City, Utah}

This work was supported by research grants from the National Institutes of Health, U. S. Public Health Service.

Find articles by Tyler, F. in: PubMed | Google Scholar

Published in Volume 34, Issue 4 on April 1, 1955
J Clin Invest. 1955;34(4):565–580. https://doi.org/10.1172/JCI103105.
© 1955 The American Society for Clinical Investigation

Published April 1, 1955 - Version history