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. 2017 Jun 5;18:63. doi: 10.1186/s12881-017-0424-5

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© The Author(s). 2017

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. 7 — Clinical features of reported SYNE1 mutations in the all word. SNV: single nucleotide variant; AMC : Arthrogryposis multiplex congenita ; EDMD4: Emery-Dreifuss muscular dystrophy 4; SCA8: Spinocerebellar ataxia8; [4]: References [4–7, 9–13]