Diabytes
Duchenne Muscular Dystrophy News
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A new study has found that gene-editing technique can successfully put a halt to Duchenne muscular dystrophy progression.
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A gene-editing technique has shown promise in treating Duchenne muscular dystrophy (DMD), the most common and severe form of muscular dystrophy among boys which is characterised by progressive muscle degeneration and weakness.
Six children, including a 6-year-old Indian-origin boy, has been denied life-saving treatment from a rare disease due to high costs by UK's state-funded health service.
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