By-passing the nonsense mutation in the 4<sup>CV</sup> mouse model of muscular dystrophy by induced exon skipping
Background: Duchenne muscular dystrophy (DMD), a severe neuromuscular disorder, is caused by protein-truncating mutations in the dystrophin gene. Absence of functional dystrophin renders muscle fibres more vulnerable to damage and necrosis. We report antisense oligomer (AO) induced exon skipping in...
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Main Authors: | Chalermchai Mitrpant, Sue Fletcher, Patrick L. Iversen, Steve D. Wilton |
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Other Authors: | University of Western Australia |
Format: | Article |
Published: |
2018
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Online Access: | https://repository.li.mahidol.ac.th/handle/123456789/27212 |
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Institution: | Mahidol University |
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