Gene therapy for muscular dystrophy stirs hopes and controversy
Briefly

Susan and Chris Finazzo have enrolled their sons Dylan and Chase in a study of gene therapy for Duchenne muscular dystrophy.The experimental treatment is still being studied but researchers hope it may help prevent the devastating effects of the disease.Natalia de la Rosa Reyes/Susan Finazzo When Chase Finazzo was just a few years old, his parents noticed Chase was pretty clumsy.
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