CRISPR Therapeutics AG
MATERIALS AND METHODS FOR TREATMENT OF DUCHENNE MUSCULAR DYSTROPHY
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Abstract:
The present application provides materials and methods for treating a patient with Duchenne Muscular Dystrophy (DMD) both ex vivo and in vivo. In addition, the present application provides materials and methods for editing a dystrophin gene in a cell by genome editing.
Status:
Application
Type:
Utility
Filling date:
28 Oct 2016
Issue date:
12 Dec 2019