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Evaluating an allele-specific genetic therapy for congenital myopathy caused by dominant mutations in the skeletal muscle actin (ACTA1) gene
Nowak, Kristen
(Investigator 01)
Laing, Nigel
(Investigator 02)
Taylor, Rhonda
(Investigator 03)
School of Biomedical Sciences
UWA Centre for Medical Research (affiliated with the Harry Perkins Institute of Medical Research)
Overview
Project Details
Status
Finished
Effective start/end date
30/05/18
→
30/11/19
Funding
Association Francaise contre les Myopathies (AFM):
A$71,090.00
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