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| Content Provider | PubMed Central |
|---|---|
| Author | Gardner, R. J. Bobrow, M. Roberts, R. G. |
| Abstract | The protein truncation test (PTT) is a mutation-detection method that monitors the integrity of the open reading frame (ORF). More than 60% of cases of Duchenne muscular dystrophy (DMD) result from gross frame-shifting deletions in the dystrophin gene that are detectable by a multiplex PCR system. It has become apparent that virtually all of the remaining DMD mutations also disrupt the translational reading frame, making the PTT a logical next step toward a comprehensive strategy for the identification of all DMD mutations. We report here a pilot study involving 22 patients and describe the mutations characterized. These constitute 12 point mutations or small insertions/deletions and 4 gross rearrangements. We also have a remaining five patients in whom there does not appear to be a mutation in the ORF. We believe that reverse-transcription--PCR/PTT is an efficient method by which to screen for small mutations in DMD patients with no deletion. |
| Starting Page | 311 |
| File Format | |
| ISSN | 15376605 |
| e-ISSN | 15376605 |
| Journal | American Journal of Human Genetics |
| Issue Number | 2 |
| Volume Number | 57 |
| Language | English |
| Publisher Date | 1995-08-01 |
| Access Restriction | Open |
| Subject Keyword | Research in Higher Education |
| Content Type | Text |
| Resource Type | Article |
| Subject | Genetics Genetics (clinical) |
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