Gene therapy: a strategy for the treatment of inherited muscle diseases?
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Updated: Oct 3, 2026

Direct Reprogramming of Human Fibroblasts into Myoblasts to Investigate Therapies for Neuromuscular Disorders
Published on: April 3, 2021
1Human Genetics Unit, CHUL Research Center, Laval University, Ste-Foy, Quebec, Canada.
Abstract:
The emergence of new vectors of viral origin (recombinant adeno-associated viruses, second and third generation adenoviruses) and a new potential source of cells for transplantation (muscle-derived stem cells) are broadening the panel of therapeutic options for myopathies. Although the perfect gene-transfer method(s) have not yet been found, recent findings will certainly constitute a strong knowledge base for future clinical trials.
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