A synopsis of the unconjugated acidic transamination metabolites of phenylalanine in phenylketonuria
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://www.springerlink.com/index/pdf/10.1007/BF01800355
Reference40 articles.
1. Armstrong, M. D., Shaw, K. N. F. and Robinson, K. S. Studies on phenylketonuria. II. The excretion ofo-hydroxyphenylacetic acid in phenylketonuria.J. Biol. Chem. 213 (1955) 797–804
2. Armstrong, M. D. and Low, N. L. Phenylketonuria. VIII. Relation between age, serum phenylalanine level and phenylpyruvic acid excretion.Proc. Soc. Exp. Biol. Med. 94 (1957) 142–146
3. Blau, K. Aromatic acid excretion in phenylketonuria. Analysis of the unconjugated aromatic acids derived from phenylalanine.Clin. Chim. Acta 27 (1970) 5–18
4. Blau, K., Summer, G. K., Newsome, H. C., Edwards, C. H. and Mamer, O. A. Phenylalanine loading and aromatic acid excretion in normal subjects and heterozygotes for phenylketonuria.Clin. Chim. Acta 45 (1973) 197–205
5. Chalmers, R. A. and Watts, R. W. E. Quantitative studies on the urinary excretion of unconjugated aromatic acids in phenylketonuria.Clin. Chim. Acta 55 (1974) 281–294
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