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. 2019 Jun 24;14:152. doi: 10.1186/s13023-019-1125-2

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© The Author(s). 2019

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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Fig. 2 — Data entries of distinct patients with a dystrophinopathies or b SMA subdivided based on the different data sources. Data entered only by genetic institutes is displayed in light blue, data from neuromuscular centers in green and data from the patient registry in teal