Carrier frequency of F508del mutation of cystic fibrosis in medical students from Universidad del Rosario, Bogotá, Colombia
Introduction: Cystic fibrosis (CF) is the most frequent autosomical recessive disorder in Caucasian population with an incidence of in 2000 newborns. The disease is caused by mutations in the cfr gene, but the most common mutation is F508del, which accounts for 66% of CF chromosomes worldwide and a...
- Autores:
- Tipo de recurso:
- Fecha de publicación:
- 2007
- Institución:
- Universidad del Rosario
- Repositorio:
- Repositorio EdocUR - U. Rosario
- Idioma:
- eng
- OAI Identifier:
- oai:repository.urosario.edu.co:10336/23718
- Acceso en línea:
- https://repository.urosario.edu.co/handle/10336/23718
- Palabra clave:
- Phenylalanine
Transmembrane conductance regulator
Adult
Article
Colombia
Controlled study
Cystic fibrosis
Female
Gene deletion
Gene frequency
Gene mutation
Genetic screening
Heteroduplex analysis
Heterozygote detection
Human
Human experiment
Male
Medical student
Normal human
Polymerase chain reaction
Carrier
Colombia
Cystic fibrosis
Deltaf508
- Rights
- License
- Abierto (Texto Completo)