Gene therapy for muscular dystrophy raises hope and controversy

Gene remedy for muscular dystrophy raises hope and controversy

Susan and Chris Finazzo enrolled their sons Dylan and Chase in a gene remedy examine for Duchenne muscular dystrophy. The experimental therapy continues to be being studied, however researchers hope it will possibly assist forestall the devastating results of the illness. Natalia de la Rosa Reyes/Susan Finazzo cover caption toggle caption Natalia de la Rosa…

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