Correction: A novel mouse model of Duchenne muscular dystrophy carrying a multi-exonic Dmd deletion exhibits progressive muscular dystrophy and early-onset cardiomyopathy
Tatianna Wai, Ying Wong, Abdalla Ahmed, Grace Yang, Eleonora Maino, Sydney Steiman, Elzbieta Hyatt, Parry Chan, Kyle Lindsay, Nicole Wong, Diane Golebiowski, Joel Schneider, Paul Delgado-Olguín, Evgueni A. Ivakine, Ronald D. Cohn

Abstract
Genes, proteins, chemicals, diseases, species, mutations and cell lines named across the full text — each resolved to its canonical identifier and authoritative record.
Click any figure to enlarge with its caption.
Figure 1Peer Reviews
No public reviews on file for this paper yet. If you reviewed it on a platform where reviews are public (OpenReview, ICLR, NeurIPS, ICML), you can paste yours below so the community can read it here.
Videos
No videos yet. Explain this paper in a talk, walkthrough, or lecture? Add one.
Taxonomy
TopicsMuscle Physiology and Disorders · RNA Research and Splicing · RNA modifications and cancer
There was an error in Dis. Model. Mech. (2020) 13, dmm045369 (doi:10.1242/dmm.045369).
The wild-type (WT) triceps image in Fig. 4G was inadvertently duplicated and shown again as the WT gastrocnemius image. This figure has been amended to show WT gastrocnemius histological staining and the corrected panel is shown below.
The authors apologise for this error and any inconvenience it may have caused.
