Corrigendum: Translation from a DMD exon 5 IRES results in a functional dystrophin isoform that attenuates dystrophinopathy in humans and mice (Nature Medicine (2014))

Nicolas Wein, Adeline Vulin, Maria S. Falzarano, Christina Al Khalili Szigyarto, Baijayanta Maiti, Andrew Findlay, Kristin N. Heller, Mathias Uhlén, Baskar Bakthavachalu, Sonia Messina, Giuseppe Vita, Chiara Passarelli, Francesca Gualandi, Steve D. Wilton, Louise R. Rodino-Klapac, Lin Yang, Diane M. Dunn, Daniel R. Schoenberg, Robert B. Weiss, Michael T. HowardAlessandra Ferlini, Kevin M. Flanigan

Research output: Contribution to journalComment/debate

Original languageEnglish
Number of pages1
JournalNature medicine
Volume21
Issue number4
DOIs
StatePublished - Apr 1 2015
Externally publishedYes

Cite this

Wein, N., Vulin, A., Falzarano, M. S., Szigyarto, C. A. K., Maiti, B., Findlay, A., Heller, K. N., Uhlén, M., Bakthavachalu, B., Messina, S., Vita, G., Passarelli, C., Gualandi, F., Wilton, S. D., Rodino-Klapac, L. R., Yang, L., Dunn, D. M., Schoenberg, D. R., Weiss, R. B., ... Flanigan, K. M. (2015). Corrigendum: Translation from a DMD exon 5 IRES results in a functional dystrophin isoform that attenuates dystrophinopathy in humans and mice (Nature Medicine (2014)). Nature medicine, 21(4). https://doi.org/10.1038/nm0415-414b