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. 2020 Jun 15;77(8):1040. doi: 10.1001/jamaneurol.2020.2025

Error in Figure

PMCID: PMC7296448  PMID: 32539096

In the Original Investigation titled “Safety, Tolerability, and Efficacy of Viltolarsen in Boys With Duchenne Muscular Dystrophy Amenable to Exon 53 Skipping: A Phase 2 Randomized Clinical Trial,”1 published online May 26, 2020, there was an error in Figure 3. In panel C, the CINRG DNHS line should be 0.42 at the week 13 visit and 0.74 at the week 25 visit. This article was corrected online.

Reference

  • 1.Clemens PR, Rao VK, Connolly AM, et al. ; CINRG DNHS Investigators . Safety, tolerability, and efficacy of viltolarsen in boys with Duchenne muscular dystrophy amenable to exon 53 skipping: a phase 2 randomized clinical trial. JAMA Neurol. Published online May 26, 2020. doi: 10.1001/jamaneurol.2020.1264 [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from JAMA Neurology are provided here courtesy of American Medical Association

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