Duchenne Muscular Dystrophy (DMD) is a severe genetic disorder characterized by progressive muscle degeneration and weakness, primarily affecting boys. Caused by mutations in the dystrophin gene, DMD leads to the absence of dystrophin, a vital protein for muscle health. Historically, DMD has posed significant challenges for both patients and researchers, with limited treatment options focused...
English
Français
Español
Português
Deutsch
Türkçe
Dutch
Italiano
Russian
Romaian