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Aspartame loading test in PKU heterozygous individuals bearing severe and moderate mutations |
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| Authors: | da Silva L C Carvalho T S da Silva F B Pires R F Giugliani R Pereira M L |
| Affiliation: | Department of Biochemistry,;Department of Genetics, Federal University of Rio Grande do Sul, Brazil,;Medical Genetics Service, Hospital de Clínicas de Porto Alegre, RS, Brazil |
| Abstract: | |
| Keywords: | amino acid disorders aspartame carrier detection hyperphenylalaninemia phenylalanine hydroxylase phenylalanine metabolism phenylketonuria tyrosine metabolism |
| 本文献已被 PubMed 等数据库收录！ | |