Abstract | BACKGROUND: METHODS: Thirty-seven DMD or BMD patients who had known exon deletions detected by conventional multiplex PCR (conventional PCR) and nine control subjects were enrolled in this study. When a discrepancy was shown between the results of conventional PCR and DPO PCR, the multiplex ligation-dependent probe amplification (MLPA) technique was performed as a confirmation test. RESULTS: The same deletions previously identified by conventional PCR in 32 out of 37 subjects were also detected by DPO PCR. For the five subjects (13.5%) showing discrepant results between the conventional PCR and DPO PCR, MLPA was performed and its results were found to correlate better with those of DPO PCR. The discrepancies were due to false positive or false negative results of the conventional PCR. CONCLUSIONS: DPO PCR shows a high agreement of results with the conventional PCR and is considered an adequate method to be used as a primary genetic test for the diagnosis of DMD. Because of an improved accuracy, especially for determining the boundaries of DMD gene deletions, DPO PCR can be very useful as a supplement to the conventional PCR.
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Authors | Younhee Park, Juwon Kim, Jong Rak Choi, Jaewoo Song, Jong Shin Chung, Kyung A Lee |
Journal | The Korean journal of laboratory medicine
(Korean J Lab Med)
Vol. 28
Issue 5
Pg. 386-91
(Oct 2008)
ISSN: 1598-6535 [Print] Korea (South) |
PMID | 18971620
(Publication Type: Comparative Study, Evaluation Study, Journal Article)
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Chemical References |
- DMD protein, human
- DNA Primers
- Dystrophin
- Oligonucleotide Probes
- Reagent Kits, Diagnostic
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Topics |
- DNA Mutational Analysis
- DNA Primers
- Dystrophin
(genetics)
- Female
- Gene Deletion
- Genetic Testing
- Humans
- Male
- Muscular Dystrophy, Duchenne
(diagnosis, genetics)
- Nucleic Acid Amplification Techniques
- Oligonucleotide Probes
- Polymerase Chain Reaction
(methods)
- Reagent Kits, Diagnostic
- Reproducibility of Results
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