Skip to content

1 paper indexed here

We haven’t gathered this author’s papers yet. Follow them and we’ll fetch their work.

Not the right person? Other researchers publish under this name.

Review Open access Sep 2026

Duchenne Muscular Dystrophy: from Dystrophin Deficiency to Emerging Therapeutic Strategies

DMD is a severe, progressive X-linked recessive neuromuscular disorder caused by pathogenic mutations in the DMD gene, resulting in deficiency or absence of the dystrophin protein, and multidisciplinary management has improved survival and quality of life.

B. Rakesh, A. A, D. S. et al. · 0 citations

We use cookies to run the site and, with your consent, for analytics and to show ads. See our Cookie Policy.