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Wein N, Vulin A, Falzarano MS, et al. Corrigendum: Translation from a DMD exon 5 IRES results in a functional dystrophin isoform that attenuates dystrophinopathy in humans and mice. Nat Med. 2015;21(4):414doi: 10.1038/nm0415-414b.
Wein, N., Vulin, A., Falzarano, M. S., Szigyarto, C. A., 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., Howard, M. T., Ferlini, A., & 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, 21(4), 414. https://doi.org/10.1038/nm0415-414b
Wein, Nicolas, et al. "Corrigendum: Translation from a DMD exon 5 IRES results in a functional dystrophin isoform that attenuates dystrophinopathy in humans and mice." Nature medicine vol. 21,4 (2015): 414. doi: https://doi.org/10.1038/nm0415-414b
Wein N, Vulin A, Falzarano MS, Szigyarto CA, Maiti B, Findlay A, Heller KN, Uhlén M, Bakthavachalu B, Messina S, Vita G, Passarelli C, Gualandi F, Wilton SD, Rodino-Klapac LR, Yang L, Dunn DM, Schoenberg DR, Weiss RB, Howard MT, Ferlini A, Flanigan KM. Corrigendum: Translation from a DMD exon 5 IRES results in a functional dystrophin isoform that attenuates dystrophinopathy in humans and mice. Nat Med. 2015 Apr;21(4):414. doi: 10.1038/nm0415-414b. PMID: 25849273.
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