ART4 and neuromuscular disease caused by qualitative or quantitative defects of dystrophin: Differential protein expression patterns were analyzed by bioinformatics and are displayed in this report according to association with the (i) dystrophin-glycoprotein complex, (ii) the established marker signature of dystrophinopathy, (iii) excitation-contraction coupling, (iv) the annexin family, (v) the collagen family, and (vi) the extracellular matrix.