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. 2020 Feb 17;10:2721. doi: 10.1038/s41598-020-59627-7

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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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Percentage of LOF variants identified in both AD cohorts in the EDC (with high incidence of LOFs identified in the SFTP family). The empty gray boxes indicate no alteration whereas the filled gray boxes indicate alteration (LOF) present in a particular subject in that particular gene. The spatial distribution displays all the patients carrying at least a single variant in the queried genes.