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. 2021 May 21;13:90. doi: 10.1186/s13073-021-00900-3

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© The Author(s) 2021

Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data.

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Fig. 4 — Protein variants of DHX30 lead to embryonal developmental defects in zebrafish. In vivo analyses of selected DHX30 missense variants. Assessment of embryonic development after injection of DHX30 WT and mutant cDNAs in a zebrafish model. Bar graph indicating the percentage of cmcl2-GFP positive zebrafish embryos assessed 4–7 days post fertilization (dpf). The presented data are derived from three independent studies. The total number of embryos assessed are 45, 23, 21, 30, 34, 33, and 29 for WT, V556I, E948K, R493H, R725H, R785C, and R908Q, respectively. ****: significantly different from WT (****p< 0.0001; χ² test)