APC mutation analysis by chemical cleavage of mismatch and a protein truncation assay in familial adenomatous polyposis.

Overall, the causative APC mutation has been identified in only 30% of the patients with familial adenomatous polyposis (FAP) who have been included in studies reported in the literature. In order to determine the true frequency of detectable APC mutations, we set out to search exhaustively the enti...

Descripción completa

Detalles Bibliográficos
Autores principales: Prosser, J., Condie, A., Wright, M., Horn, J. M., Fantes, J. A., Wyllie, A. H., Dunlop, M. G.
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1994
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2033526/
https://www.ncbi.nlm.nih.gov/pubmed/7524601

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2033526/
https://www.ncbi.nlm.nih.gov/pubmed/7524601

Ejemplares similares