Skip to content
Advertisement

FILE - A sign for the Food and Drug Administration is displayed outside their offices in Silver Spring, Md., on Dec. 10, 2020. The first gene therapy for Duchenne muscular dystrophy received preliminary U.S. approval on Thursday, June 22, 2023, despite concerns from some government scientists about the treatment's ability to help boys with the inherited disease. (AP Photo/Manuel Balce Ceneta, File)

FILE - A sign for the Food and Drug Administration is displayed outside their offices in Silver Spring, Md., on Dec. 10, 2020. The first gene therapy for Duchenne muscular dystrophy received preliminary U.S. approval on Thursday, June 22, 2023, despite concerns from some government scientists about the treatment's ability to help boys with the inherited disease. (AP Photo/Manuel Balce Ceneta, File)

Featured Photo Galleries