Sarepta Therapeutics, Inc.
Exon skipping oligomer conjugates for muscular dystrophy
Last updated:
Abstract:
Antisense oligomers complementary to a selected target site in the human dystrophin gene to induce exon 52 skipping are described.
Status:
Grant
Type:
Utility
Filling date:
30 May 2018
Issue date:
1 Sep 2020