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. 2011 Nov 18;134(12):3544–3556. doi: 10.1093/brain/awr291

Figure 2.

Figure 2

Representative immunohistochemistry images of dystrophin and dystrophin-associated proteins in patients with Becker muscular dystrophy (BMD) with in-frame deletions. Unfixed, frozen transverse muscle sections (7 µm) from control, Duchenne muscular dystrophy (DMD) and Becker muscular dystrophy (Patients 8, 11 and 16 are shown) patients were immunolabelled with MANDYS106 (M106, exon 43) and Dys2 (last 17 amino acids of the C-terminus) antibodies against dystrophin and with antibodies against α-sarcoglycan (ASG), β-dystroglycan (BDG), neuronal nitric oxide synthase (nNOS) and β-spectrin (SP). Scale bar = 20 µm.