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![RNA antisense and silencing strategies using synthetic drugs for rare muscular and neuromuscular diseases](https://image.oaes.cc/d14b3448-0c17-4ab2-aa69-f595b3de197d/5782.fig.8.jpg)
Figure 8. A: Exons 43 to 53 of the integral dystrophin gene. B: In grey, the group of exons whose concomitant deletion could, in theory, lead to a shortened functional or semi-functional dystrophin protein comprising only the protein encoded by the exons in blue, and allowing to skip mutated Exon 51.