Phenylalanine metabolites in treated phenylketonuric children
- Author
- MICHALS, K1 ; LOPUS, M; GASHKOFF, P; MATALON, R
[1] Univ. Illinois, dep. nutrition medical dietetics, Chicago IL, United States - Conference name
- Society for the study of inborn errors of metabolism. Annual symposium. 23 (1985)
- Source
Journal of inherited metabolic disease. 1986, Vol 9, pp 212-214 ; suppl. 2 ; ref : 6 ref
- CODEN
- JIMDDP
- ISSN
- 0141-8955
- Scientific domain
- Genetics; Nutrition, obesity, metabolic disorders
- Publisher
- Springer, Dordrecht
- Publication country
- Netherlands
- Document type
- Conference Paper
- Language
- English
- Keyword (fr)
- Aminoacidopathie Homme Maladie héréditaire Métabolisme pathologie Métabolite Phénylalanine Phénylcétonurie
- Keyword (en)
- Aminoacid disorder Human Genetic disease Metabolic diseases Metabolite Phenylalanine Phenylketonuria
- Keyword (es)
- Aminoacidos alteracion Hombre Enfermedad hereditaria Metabolismo patologia Metabolito Fenilalanina Fenilcetonuria
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B22 Metabolic diseases / 002B22D Errors of metabolism / 002B22D01 Aminoacid disorders
- Discipline
- Metabolic diseases
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 7958045
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.1007/BF01799708 
https://dx.doi.org/10.1007/BF01799708
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