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. 2022 Jun 13;93(9):919–929. doi: 10.1136/jnnp-2021-328586

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© Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.

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Genetic–pathological–clinical correlations in CBS. Font size reflects the frequency of each mutation or pathological diagnosis. Note that the majority of pathologies are sporadic; only a small subset of cases has gene mutations indicated. AD, Alzheimer’s disease; CBD, corticobasal degeneration; CBS, corticobasal syndrome; CJD, Creutzfeldt-Jakob disease; FTLD-FUS, frontotemporal lobar degeneration with fused-in-sarcoma pathology; FTLD-TDP, frontotemporal lobar degeneration with TDP-43 inclusions; LBD, Lewy body disease; PSP, progressive supranuclear palsy.