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- The US Food and Drug Administration has given the green light for the first gene therapy that treats a rare form of muscular dystrophy to be used in most people who have the disease and a certain genetic mutation.www.cnn.com/2024/06/20/health/fda-gene-therapy-duchenne-muscular-dystrop…
FDA expands approval of first gene therapy for rare form of …
Muscular dystrophy patients get first gene therapy - NPR
WEBJun 22, 2023 · The Food and Drug Administration approved the first gene therapy for Duchenne muscular dystrophy, but limited access to those …
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