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