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. 2022 May 12;17:197. doi: 10.1186/s13023-022-02340-7

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© The Author(s) 2022

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. 2 — Distribution of the phenotypes of 194 North African families with non-syndromic IRD. According to disease categories in the center chart, and within each category in the outer charts. ACHM: achromatopsia, ARB: autosomal recessive bestrophinopathy, BVMD: Best vitelliform macular dystrophy, CHM: choroideremia, CRD: cone-rod dystrophy, CNSB: congenital stationary night blindness, EORD: early onset retinal dystrophy, ESCD: enhanced S-cone syndrome, LCA: Leber congenital amaurosis, OCA: oculocutaneous albinism, RP: retinitis pigmentosa, RPA: retinitis punctata albescens, STGD: Stargardt disease