A cystic fibrosis patient who is homozygous for the G85E mutation has very mild disease.

Author:

Chalkley G,Harris A

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference9 articles.

1. Identification of the cystic fibrosis gene: genetic analysis;Kerem, B.S.; Rommens, J.M.; Buchanan, J.A.;Science,1989

2. Multiple authors. Worldwide survey of the delta 508 mutation. Report from the Cystic Fibrosis Genetic Analysis Consortium;Am Hum Genet,1990

3. Gradient of distribution in Europe of the major CF mutation and of its haplotype;authors, Multiple;Hum Genet,1990

4. The relation between genotype and phenotype in cystic fibrosis: analysis of the most common mutation (AF508);Kerem, E.; Corey, M.; Kerem, B.S.;N EnglJ Med,1990

5. Pancreatic function and gene deletion AF508 in cystic fibrosis;Borgo, G.; Mastella, G.; Gasparini, P.; Zorzanello, A.; Doro, R.; Pignatti, P.F.;Med Genet,1990

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