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10 months ago

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Muscular dystrophy breakthrough: FDA approves first-ever gene therapy for rare children's disease

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Muscular dystrophy breakthrough: FDA approves first-ever gene therapy for rare children's disease

The FDA has approved the first gene therapy for the treatment of Duchenne muscular dystrophy (DMD) in children 4-5 years of age. Get the details on how Elevidys could help pediatric patients.

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health baby motherhood children fda public health public safety united states usa dystrophy gene therapy

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Muscular dystrophy breakthrough: FDA approves first-ever gene therapy for rare children's disease

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Muscular dystrophy breakthrough: FDA approves first-ever gene therapy for rare children's disease

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