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New gene therapy approach shows promise for Duchenne muscular dystrophy - EurekAlert
New gene therapy approach shows promise for Duchenne muscular dystrophy
CRISPR-Cas3 gene editing system restores dystrophin function in stem cells derived from patients with Duchenne muscular dystrophy
Blocking an ion channel improves muscle function and survival in mice with severe Duchenne muscular dystrophy
Daily steroids safe and slows progression of duchenne muscular dystrophy, study suggests
Cell treatment slows disease in Duchenne muscular dystrophy patients
Piezo1 possible key to supporting muscle regeneration in Duchenne Muscular Dystrophy
Cellular therapy improves signs and symptoms of Duchenne muscular dystrophy
New 'cocktail' drug could benefit up to 45 per cent of patients with Duchenne muscular dystrophy
Steroid treatments for Duchenne muscular dystrophy may depend on the clock
New gene editing strategies developed for Duchenne muscular dystrophy
New discovery could lead to therapies for patients with Duchenne muscular dystrophy
Digging deep for differences in Duchenne muscular dystrophy
