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. 2018 Dec 3;9:1402. doi: 10.3389/fphar.2018.01402

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Copyright © 2018 Kameyama, Ohuchi, Funato, Ando, Inagaki, Sato, Seki, Kawase, Tsuruma, Nishino, Nakamura, Shimazawa, Saito, Takeda, Kaneko and Hara.

This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

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Genetic diagnosis of Duchenne muscular dystrophy (DMD) patients (DMD01 and 02) used in this study. (A–C) The Multiplex ligation-dependent probe amplification analysis of the DMD patients (DMD01 and 02) in this study. The exons 42 and 43 deletion were found in DMD01, but no deletion and duplication in DMD02. DMD02 showed c.4545_4549delGAAGT, p.Lys1516^∗ in exon 33.