fig8

RNA antisense and silencing strategies using synthetic drugs for rare muscular and neuromuscular diseases

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.

Rare Disease and Orphan Drugs Journal
ISSN 2771-2893 (Online)
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