Translation from a DMD exon 5 IRES results in a functional dystrophin isoform that attenuates dystrophinopathy in humans and mice

Overview of attention for article published in Nature Medicine, August 2014

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Ribosome profiling data from Wein et al. 2014 (https://t.co/eQFiBMvudz) is now in GWIPS-viz under hg38 #riboseq

A potential therapeutic approach for a subset of patients with DMD @NatureMedicine @CAGC_ACCG http://t.co/fW59hnj3x1

Alternative translation initiation in DMD gene helps in human cells + mouse model of Duchenne muscular dystrophy http://t.co/7rsLU5lSsU

A potential therapeutic approach for a subset of patients with DMD @NatureMedicine @CAGC_ACCG http://t.co/fW59hnj3x1

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