Detection by Phenylalanine Tolerance Tests of Heterozygous Carriers of Phenylketonuria-Reference-Cited by-同舟云学术

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Detection by Phenylalanine Tolerance Tests of Heterozygous Carriers of Phenylketonuria

Published:1956-12 Issue:4544 Volume:178 Page:1239-1240
ISSN:0028-0836
Container-title:Nature
language:en
Short-container-title:Nature

Author:

HSIA DAVID Y.-Y.,DRISCOLL KATHLEEN W.,TROLL WALTER,EUGENE KNOX W.

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/1781239a0.pdf

Reference6 articles.

1. Pauling, L., “Harvey Lectures”, 49, 216 (1953–54).

2. Knox, W. E., Bull. Tufts-N.E. Med. Center, 2, 1 (1956).

3. Jervis, G. A., Proc. Soc. Exp. Biol. and Med., 82, 514 (1953).

4. Jervis, G. A., Res. Pub. Assoc. Nerv. Ment. Dis., 33, 259 (1954).

5. Udenfriend, S., and Cooper, J. R., J. Biol. Chem., 203, 953 (1953).

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1. Phenylalanine Monitoring via Aptamer-Field-Effect Transistor Sensors;ACS Sensors;2019-10-21

2. Phenylketonuria (PKU);Genes, Brain Function, and Behavior;2019

3. Phenylalanine and Tyrosine Metabolism Analysis in Heterozygotes for Phenylketonuria and in Healthy Individuals;Journal of Inborn Errors of Metabolism and Screening;2015-02-18

4. Diagnosis, classification, and genetics of phenylketonuria and tetrahydrobiopterin (BH4) deficiencies;Molecular Genetics and Metabolism;2011-01

5. Heterozygous carriers in the relatives of a case of phenylketonuria;Hereditas;2009-02-12

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