Molecular basis of phenotypic heterogeneity in phenylketonuria
- Author
- OKANO, Y; EISENSMITH, R; WOO, S. L. C; GUÊTTLER, F; LICHTER-KONECKI, U; KONECKI, D. S; TREFZ, F. K; DASOVICH, M; WANG, T; HENRIKSEN, K; LOU, H
Howard Hughes medical inst., Baylor coll. medicine, Houston, United States - Source
The New England journal of medicine. 1991, Vol 324, Num 18, pp 1232-1238, 7 p ; ref : 41 ref
- CODEN
- NEJMAG
- ISSN
- 0028-4793
- Scientific domain
- General medicine general surgery
- Publisher
- Massachusetts Medical Society, Boston, MA
- Publication country
- United States
- Document type
- Article
- Language
- English
- Keyword (fr)
- Aminoacidopathie Génotype Homme Maladie héréditaire Métabolisme pathologie Phénotype Phénylcétonurie
- Keyword (en)
- Aminoacid disorder Genotype Human Genetic disease Metabolic diseases Phenotype Phenylketonuria
- Keyword (es)
- Aminoacido alteración Genotipo Hombre Enfermedad hereditaria Metabolismo patología Fenotipo 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
- 19632295
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
10.1056/NEJM199105023241802 
https://dx.doi.org/10.1056/NEJM199105023241802
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