Aspartame loading test in PKU heterozygous individuals bearing severe and moderate mutations-Reference-Cited by-同舟云学术

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Aspartame loading test in PKU heterozygous individuals bearing severe and moderate mutations

Published:2000-07 Issue:1 Volume:58 Page:86-88
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clinical Genetics

Author:

Santana da Silva Luiz Carlos,Carvalho Tiago Santos,Da Silva Fernanda B.,Flores Pires Ricardo,Giugliani Roberto,Saraiva Pereira Maria Luiza

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1034/j.1399-0004.2000.580118.x/fullpdf

Reference13 articles.

1. PAH Mutation Analysis Consortium Database 1997. Prototype for relational locus-specific mutation databases;Nowacki;Nucleic Acids Res,1998

2. A European multicenter study for phenylalanine hydroxylase deficiency: classification of 105 mutations and a general system for genotype-based prediction of metabolic phenotype;Guldberg;Am J Hum Genet,1998

3. Detection of heterozygous carriers for phenylketonuria by a L-[2H5] phenylalanine stable isotope loading test;Lehmann;Clin Chim Acta,1984

4. Heterozygous carriers of classical phenylketonuria in a sample of the Turkish population: detection by a spectrofluorimetric method;Güneral;J Inher Metab Dis,1991

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Accidental Consumption of Aspartame in Phenylketonuria: Patient Experiences;Nutrients;2021-02-23

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

3. Aspartame: A Safety Evaluation Based on Current Use Levels, Regulations, and Toxicological and Epidemiological Studies;Critical Reviews in Toxicology;2007-01

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