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The origin of the major cystic fibrosis mutation (delta F508) in European populations
N Morral, J Bertranpetit, X Estivill, V Nunes, T Casals, J Gimenez, A Reis, R Varon-Mateeva, M Jr Macek, L Kalaydjieva
Language English Country United States
Document type Research Support, Non-U.S. Gov't
Grant support
PL215
MZ0
CEP Register
PubMed
7920636
Knihovny.cz E-resources
- MeSH
- Biological Evolution MeSH
- Time Factors MeSH
- Cystic Fibrosis * genetics MeSH
- Genetic Variation MeSH
- Genetic Markers MeSH
- Haplotypes MeSH
- Humans MeSH
- Mutation * MeSH
- Genetics, Population MeSH
- Repetitive Sequences, Nucleic Acid MeSH
- Check Tag
- Humans MeSH
- Publication type
- Research Support, Non-U.S. Gov't MeSH
- Geographicals
- Europe MeSH
delta F508 is the most frequent cystic fibrosis (CF) mutation and accounts for approximately 70% of CF chromosomes worldwide. Three highly polymorphic microsatellite markers have been used to study the origin and evolution of delta F508 chromosomes in Europe. Haplotype data demonstrate that delta F508 occurred more than 52,000 years ago, in a population genetically distinct from any present European group, and spread throughout Europe in chronologically distinct expansions, which are responsible for the different frequencies of delta F508 in Europe.
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- $a delta F508 is the most frequent cystic fibrosis (CF) mutation and accounts for approximately 70% of CF chromosomes worldwide. Three highly polymorphic microsatellite markers have been used to study the origin and evolution of delta F508 chromosomes in Europe. Haplotype data demonstrate that delta F508 occurred more than 52,000 years ago, in a population genetically distinct from any present European group, and spread throughout Europe in chronologically distinct expansions, which are responsible for the different frequencies of delta F508 in Europe.
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