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. 2018 Jul 5;8:10176. doi: 10.1038/s41598-018-27951-8

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© The Author(s) 2018

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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Identification of casual variants in bestrophinopathy families. (a) Flowchart depicting the analysis of exome data from bestrophinopathy patients and their relatives. (b) Pedigrees of four bestrophinopathy families analyzed in this study. Candidate variants identified in each family is shown. White circles - unaffected females; white squares - unaffected male; filled circles - affected females; filled squares - affected males. Number within circle/square indicates that the sample was sequenced.