A termination mutation prevalent in Norwegian haplotype 7 phenylketonuria genes
- Author
- APOLD, J; EIKEN, H. G; ODLAND, E; FREDRIKSEN, A; BAKKEN, A; LORENS, J. B; BOMAN, H
Univ. Bergen, dep. medical genetics, Bergen, Norway - Source
American journal of human genetics. 1990, Vol 47, Num 6, pp 1002-1007 ; ref : 19 ref
- Publisher
- University of Chicago Press, Chicago, IL
- Publication country
- United States
- Document type
- Article
- Language
- English
- Keyword (fr)
- Enfant Exploration Gène Génétique Haplotype Mutation Métabolisme pathologie Phénylcétonurie Polymorphisme longueur fragment restriction Réaction chaîne polymérase Phénylalanine hydroxylase Norvège Homme Europe
- Keyword (en)
- Child Exploration Gene Genetics Haplotype Mutation Metabolic diseases Phenylketonuria Restriction fragment length polymorphism Polymerase chain reaction Norway Human Europe
- Keyword (es)
- Niño Exploración Gen Genética Haplotipo Mutación Metabolismo patología Fenilcetonuria Polimorfismo longitud fragmento restricción Reacción cadena polimerasa Noruega Hombre Europa
- Classification
- Discipline
- Metabolic diseases
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 5367433
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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