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32) Kameya S, Araki E, Katsuki M, et al. Dp260 disrupted mice revealed prolonged implicit time of the b-wave in ERG and loss of accumulation of beta-dystroglycan in the outer plexiform layer of the retina. Hum Mol Genet. 1997; 6: 2195-203
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34) Yokota T, Pistilli E, Duddy W, et al. Potential of oligonucleotide-mediated exon-skipping therapy for Duchenne muscular dystrophy. Expert Opin Biol Ther. 2007; 7: 831-42
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35) Nakamura A, Yoshida K, Fukushima K, et al. Follow-up of three cases with a large in-frame deletion of exons 45-55 in the Duchenne muscular dystrophy (DMD) Gene. J Clin Neurosci. 2008; 15: 757-63
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36) Beroud C, Tuffery-Giraud S, Matsuo M, et al. Multiexon skipping leading to an artificial DMD protein lacking amino acids from exons 45 through 55 could rescue up to 63% of patients with Duchenne muscular dystrophy. Hum Mutat. 2007; 28: 196-202
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