Transient hyperammonaemia
- Author
- HARRIS, D. J1 ; SIEGEL, C; BASKA, R. E
[1] Univ. Missouri, children's Mercy hosp., sect. genetics, Kansas City MO 64108, United States - Source
Journal of inherited metabolic disease. 1987, Vol 10, Num 3 ; 269 ; ref : 2 ref
- 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)
- Acidurie Aminoacidopathie Homme Hyperammoniémie Intolérance Lysine Maladie héréditaire Métabolisme pathologie Ornithine Protéine Transitoire Protéine dibasique
- Keyword (en)
- Aciduria Aminoacid disorder Human Dibasic protein Hyperammonemia Intolerance Lysine Genetic disease Metabolic diseases Ornithine Proteins Transitory
- Keyword (es)
- Aciduria Aminoacido alteración Hombre Hiperamonemia Intolerancia Lisina Enfermedad hereditaria Metabolismo patología Ornitina Proteina Transitorio
- 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
- 7544374
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/BF01800074 
https://dx.doi.org/10.1007/BF01800074
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