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. 2021 Jun 19;10(2):481–490. doi: 10.1007/s40119-021-00226-6

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© The Author(s) 2021

Open Access This article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial 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-nc/4.0/.

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Fig. 1 — Phenotypic categories of patients from Bulgaria and Italy with symptomatic ATTRv Glu89Gln amyloidosis at enrollment in THAOS (data cutoff, January 6, 2020). ATTRv Glu89Gln amyloidosis ATTRv amyloidosis associated with the Glu89Gln variant; THAOS Transthyretin Amyloidosis Outcomes Survey