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Development of antisense oligonucleotide drugs to supress expression of the DUX4 protein as a therapy for fascioscapulohumeral muscular dystrophy (FSHD)
Development of antisense oligonucleotide drugs to supress expression of the DUX4 protein as a therapy for fascioscapulohumeral muscular dystrophy (FSHD)
Project
:
Research
Dickson, George
(PI)
Department of Biological Sciences
Centre of Gene and Cell Therapy
Status
Finished
Effective start/end date
1/08/14
→
31/07/18
ID: 21724997
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