Identification of seven rather infrequent and one novel CFTR mutation in the Belgian population
- Author
- HUI TENG1 ; CUPPENS, H1 ; DE BOECK, C; CASSIMAN, J.-J1
[1] Univ. Leuven, cent. human genetics, 3000 Leuven, Belgium - Source
Human molecular genetics (Print). 1994, Vol 3, Num 12, pp 2249-2250 ; ref : 10 ref
- Publisher
- Oxford University Press, Oxford
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Gène Génétique Homme Mucoviscidose Mutation Appareil digestif pathologie Appareil respiratoire pathologie Maladie héréditaire Pancréas pathologie
- Keyword (en)
- Gene Genetics Human Cystic fibrosis Mutation Digestive diseases Respiratory disease Genetic disease Pancreatic disease
- Keyword (es)
- Gen Genética Hombre Mucoviscidosis Mutación Aparato digestivo patología Aparato respiratorio patología Enfermedad hereditaria Páncreas patología
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B13 Gastroenterology. Liver. Pancreas. Abdomen / 002B13C Liver. Biliary tract. Portal circulation. Exocrine pancreas / 002B13C03 Other diseases. Semiology
- Discipline
- Gastroenterology. Liver. Pancreas. Abdomen
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 3326513
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
10.1093/hmg/3.12.2249 
https://dx.doi.org/10.1093/hmg/3.12.2249
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