Özet
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.
| Orijinal dil | İngilizce |
|---|---|
| Makale numarası | 1241 |
| Dergi | Genes |
| Hacim | 13 |
| Basın numarası | 7 |
| DOI'lar | |
| Yayın durumu | Yayınlandı - Tem 2022 |
| Harici olarak yayınlandı | Evet |
Parmak izi
Current Outline of Exon Skipping Trials in Duchenne Muscular Dystrophy' araştırma başlıklarına git. Birlikte benzersiz bir parmak izi oluştururlar.Bundan alıntı yap
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