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Updated: Sep 29, 2026

Characterizing Exon Skipping Efficiency in DMD Patient Samples in Clinical Trials of Antisense Oligonucleotides
Published on: May 7, 2020
[Application of PCR technique in genetic diagnosis of Duchenne/Becker muscular dystrophy]
Yong-Mei Liu1, Zhi-Chun Feng, Zhen-Wei Fang
1Department of Pediatrics, Zhujiang Hospital, First Military Medical University, Guangzhou 510282, China.
Objective:
To study the application of PCR technique in genetic detection of Duchenne/Becker muscular dystrophy (DMD/BMD).
Methods:
A multiple PCR system is established according to the multiple sites of DMD/BMD exon deletion. Under different PCR conditions, multiple exon deletions, single-strand conformation polymorphism, allopolyploid, chain labeling, restriction fragment length polymorphism and microsatellite phenomenon were examined in 23 DMD/BMD patients and 57 suspected carriers of these genes.
Results:
Fourteen of the 23 DMD/BMD patients were identified as having gene deletion, with another 2 carried gene duplicates. Forty female relatives of these 23 DMD/BMD patients were diagnosed as carriers of the genes.
Conclusion:
This PCR system can be applied in detecting gene mutation of DMD/BMD, screening the carriers and in appropriate genealogical analysis of the patients with DMD/BMD.
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