There are many challenges in finding an effective, long-lasting and universal cure for the whole cohort of patients with Duchenne muscular dystrophy (DMD). The discovery of H19 lncRNA as a stabiliser of dystrophin may prove to be the missing link to the success of various rescue therapies proposed for treating DMD.
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M.A.R. is a Founder and CSO of Satellos Bioscience. M.R. declares no competing interests.
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Ritso, M., Rudnicki, M.A. H19 lncRNA to dystrophin’s rescue. Nat Cell Biol 22, 1289–1290 (2020). https://doi.org/10.1038/s41556-020-00598-2
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DOI: https://doi.org/10.1038/s41556-020-00598-2
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