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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.

Authors :
Wein, Nicolas
Vulin, Adeline
Falzarano, Maria S
Szigyarto, Christina Al-Khalili
Maiti, Baijayanta
Findlay, Andrew
Heller, Kristin N
Uhlén, Mathias
Bakthavachalu, Baskar
Messina, Sonia
Vita, Giuseppe
Passarelli, Chiara
Gualandi, Francesca
Wilton, Steve D
Rodino-Klapac, Louise R
Yang, Lin
Dunn, Diane M
Schoenberg, Daniel R
Weiss, Robert B
Howard, Michael T
Source :
Nature Medicine; Apr2015, Vol. 21 Issue 4, p414-414, 1p
Publication Year :
2015

Abstract

A correction to the article "Translation from a DMD exon 5 IRES results in a functional dystrophin isoform that attenuates dystrophinopathy in humans and mice" that was published in the August, 25, 2014 issue, after correction, is presented.

Subjects

Subjects :
NUCLEOTIDES
DYSTROPHIN

Details

Language :
English
ISSN :
10788956
Volume :
21
Issue :
4
Database :
Complementary Index
Journal :
Nature Medicine
Publication Type :
Academic Journal
Accession number :
101963330
Full Text :
https://doi.org/10.1038/nm0415-414b