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Cell Press, Molecular Therapy - Methods and Clinical Development, (26), p. 279-293, 2022

DOI: 10.1016/j.omtm.2022.07.005

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Systemic delivery of an AAV9 exon-skipping vector significantly improves or prevents features of Duchenne muscular dystrophy in the Dup2 mouse

This paper is made freely available by the publisher.
This paper is made freely available by the publisher.

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