Identification of a CGTR frameshift mutaiton (1013 delAA) in trans to ΔF508 in a pancreatic sufficient cystic fibrosis patient
- Author
- NASR, S. Z1 ; STRONG, T. V; COLLINS, F. S
[1] Univ. Michigan, dep. pediatrics, Ann Arbor MI 48109, United States - Source
Human molecular genetics (Print). 1994, Vol 3, Num 11, pp 2063-2064 ; ref : 20 ref
- Publisher
- Oxford University Press, Oxford
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Gène Génétique Homme Mucoviscidose Mutation cadre lecture Appareil digestif pathologie Appareil respiratoire pathologie Maladie héréditaire Pancréas pathologie
- Keyword (en)
- Gene Genetics Human Cystic fibrosis Frameshift mutation Digestive diseases Respiratory disease Genetic disease Pancreatic disease
- Keyword (es)
- Gen Genética Hombre Mucoviscidosis Mutación frameshift 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
- 3297145
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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