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,...

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Detalles Bibliográficos
Autores Principales: Jay L.M., Mateus H., Fonseca-Mendoza, Dora Janeth, Restrepo C.M., Keyeux G.
Formato: Artículo (Article)
Lenguaje:Inglés (English)
Publicado: 2006
Materias:
Acceso en línea:https://repository.urosario.edu.co/handle/10336/23713