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. Howard; Alessandra Ferlini; Kevin M. Flanigan

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

Wein N
Vulin A
Falzarano M
et al.

Nature Medicine

DOI: 10.1038/nm0415-414b

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Wein, N., Vulin, A., Falzarano, M. S., Szigyarto, C. A. K., Maiti, B., Findlay, A., … Flanigan, K. M. (2015, April 1). 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. Nature Publishing Group. https://doi.org/10.1038/nm0415-414b

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

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