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. 2020 Jun 12;10:9531. doi: 10.1038/s41598-020-65737-z

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© The Author(s) 2020

Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.

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Pedigrees of 13 Japanese families with inherited retinal disorder harbouring CRX variants. The solid squares and circles (men and women, respectively) represent the affected subjects, and the white icons represent the unaffected family members. The slash symbol shows deceased individuals. The generation number is noted on the left. The proband is marked by an arrow, and the clinically investigated individuals are indicated by a cross.