| Literature DB >> 1551658 |
L Picci1, F Anglani, M Scarpa, F Zacchello.
Abstract
We have developed a simple rapid DNA screening test that allows us simultaneously to analyze seven CF mutations (delta F508, R347P, S549N, G551D, R553X, R334W, 444delA) that together account for about 60% of all CF mutations in the Italian population. It consists of three steps: multiplex polymerase chain reaction (PCR) amplification of exons 4, 7, 10 and 11; restriction endonuclease digestion of the PCR products; and vertical polyacrylamide gel electrophoresis analysis. We have used our multiplex assay for analyzing 15 CF chromosomes (non delta F508) and have found 3 cases of the R553X mutation; the latter have been confirmed by amplification and digestion of exon 11.Entities:
Mesh:
Substances:
Year: 1992 PMID: 1551658 DOI: 10.1007/bf00219343
Source DB: PubMed Journal: Hum Genet ISSN: 0340-6717 Impact factor: 4.132