Survey of CF mutations in the clinical laboratory

BACKGROUND: Since it is impossible to sequence the complete CFTR gene routinely, clinical laboratories must rely on test systems that screen for a panel of the most frequent mutations causing disease in a high percentage of patients. Thus, in a cohort of 257 persons that were referred to our laborat...

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Detalles Bibliográficos
Autores principales: Huber, Klaus Roland, Mirkovic, Borka, Nersesian, Rhea, Myers, Angela, Saiki, Randall, Bauer, Kurt
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2002
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC138794/
https://www.ncbi.nlm.nih.gov/pubmed/12437773
http://dx.doi.org/10.1186/1472-6890-2-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC138794/
https://www.ncbi.nlm.nih.gov/pubmed/12437773
http://dx.doi.org/10.1186/1472-6890-2-4

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