Abstract
Molecular treatments for Duchenne muscular dystrophy (DMD) are already in clinical practice. One particular means is exon skipping, an approach which has more than 15 years of background. There are several promising clinical trials based on earlier works. The aim is to be able to initiate the production of enough dystrophin to change the rate of progression and create a clinical shift towards the better. Some of these molecules already have received at least conditional approval by health authorities; however, we still need new accumulating data.
| Original language | English |
|---|---|
| Article number | 1241 |
| Journal | Genes |
| Volume | 13 |
| Issue number | 7 |
| DOIs | |
| Publication status | Published - Jul 2022 |
| Externally published | Yes |
Keywords
- DMD
- antisense oligonucleotide
- clinical trials
- exon skipping
- therapy
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