Atypical phenylketonuric heterozygote
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology and Child Health
Reference33 articles.
1. Inherited metabolic disorders: Errors of phenylalanine and tyrosine metabolism;Woolf;Advances Clin. Chem.,1963
2. Atypical phenylketonuria in sisters with normal offspring;Woolf;Lancet,1961
3. Studies on phenylketonuria: The excretion of o-hydroxyphenylacetic acid in phenylketonuria;Armstrong;J. Biol. Chem.,1955
4. O-hydroxyphenylacetic acid excretion in phenylalanine tolerance test for carriers;Cullen;Proc. Soc. Exper. Biol. & Med.,1958
5. The development of biochemical abnormalities in phenylketonuric infants;Armstrong,1961
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1. Phenylketonuria 1967;Developmental Medicine & Child Neurology;2008-11-12
2. The Measurement of Phenylalanine and Tyrosine in Blood;Methods of Biochemical Analysis;2006-10-31
3. Hyperphenylalaninemia with defective transamination;Clinica Chimica Acta;1983-07
4. Plasma and erythrocyte concentrations of free amino acids in adult humans administered abuse doses of aspartame;Journal of Toxicology and Environmental Health;1981-02
5. Plasma phenylalanine levels in phenylketonuric heterozygous and normal adults administered aspartame at 34 mg/kg body weight;Toxicology;1981-01
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