PCR-heteroduplex by grouping: Rapid screening carrier method for cystic fibrosis F508del mutation in Colombia
Background: Cystic fibrosis (CF) is the most frequent autosomal recessive disorder in the Caucasian population with an incidence of 1 in 2,500 newborns. More than 1,300 mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene that causes CF have been described. However, mutat...
- Autores:
- Tipo de recurso:
- Fecha de publicación:
- 2006
- Institución:
- Universidad del Rosario
- Repositorio:
- Repositorio EdocUR - U. Rosario
- Idioma:
- eng
- OAI Identifier:
- oai:repository.urosario.edu.co:10336/23713
- Acceso en línea:
- https://repository.urosario.edu.co/handle/10336/23713
- Palabra clave:
- Transmembrane conductance regulator
Article
Blood sampling
Colombia
Controlled study
Cost effectiveness analysis
Cystic fibrosis
Diagnostic accuracy
Diagnostic value
Disease association
Disease carrier
Early diagnosis
Gene mutation
Genetic counseling
Genetic screening
Genetic susceptibility
Heteroduplex analysis
Heterozygote
Human
Incidence
Major clinical study
Morbidity
Mortality
Polymerase chain reaction
Reliability
Reproducibility
Risk reduction
Screening test
Sensitivity and specificity
Cftr
Colombia
Cystic fibrosis
Genetic screening
Heteroduplex analysis
- Rights
- License
- Abierto (Texto Completo)