"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...

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Detalles Bibliográficos
Autores Principales: Mateus H.E., Fonseca-Mendoza, Dora Janeth, Sanchez L.S., Peñaloza I.F., Forero D.V., Perdomo P.A., Quiasua D.C., Ramírez A., Montoya L.C., Pérez L.A., Amado H.P., Molano J.A., Amaya S.A., Duran M.H., Cárdenas V.C., Guevara K., Parga D.A., Esparrogosa C.L.
Formato: Artículo (Article)
Lenguaje:Inglés (English)
Publicado: 2007
Materias:
Acceso en línea:https://repository.urosario.edu.co/handle/10336/23718