A synopsis of the unconjugated acidic transamination metabolites of phenylalanine in phenylketonuria
- Author
- LANGENBECK, U; BEHBEHANI, A; MENCH-HOINOWSKI, A
Univ. Göttingen, inst. human genetics, Göttingen 3400, Germany - Source
Journal of inherited metabolic disease. 1992, Vol 15, Num 1, pp 136-144 ; ref : 2 p
- CODEN
- JIMDDP
- ISSN
- 0141-8955
- Scientific domain
- Genetics; Nutrition, obesity, metabolic disorders
- Publisher
- Springer, Dordrecht
- Publication country
- Netherlands
- Document type
- Article
- Language
- English
- Keyword (fr)
- Adolescent Dosage Enfant Forme libre Maladie héréditaire Métabolisme pathologie Métabolite Phénylalanine Phénylcétonurie Transamination Homme
- Keyword (en)
- Adolescent Assay Child Free form Genetic disease Metabolic diseases Metabolite Phenylalanine Phenylketonuria Transamination Human
- Keyword (es)
- Adolescente Dosificación Niño Forma libre Enfermedad hereditaria Metabolismo patología Metabolito Fenilalanina Fenilcetonuria Transaminación Hombre
- 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
- 5266869
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/BF01800355 
https://dx.doi.org/10.1007/BF01800355
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