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. 2021 Jan 30;141(3):467–468. doi: 10.1007/s00401-021-02262-x

Correction to: Diverse, evolving conformer populations drive distinct phenotypes in frontotemporal lobar degeneration caused by the same MAPT‑P301L mutation

Nathalie Daude 1, Chae Kim 2, Sang‑Gyun Kang 1, Ghazaleh Eskandari‑Sedighi 1,7, Tracy Haldiman 2, Jing Yang 1, Shelaine C Fleck 1,7, Erik Gomez‑Cardona 7, Zhuang Zhuang Han 1,7, Sergi Borrego‑Ecija 4, Serene Wohlgemuth 1, Olivier Julien 7, Holger Wille 1,7, Laura Molina‑Porcel 5, Ellen Gelpi 4,6, Jiri G Safar 2,3,, David Westaway 1,7,
PMCID: PMC8025258  PMID: 33515276

Correction to: Acta Neuropathologica (2020) 139:1045–1070 10.1007/s00401-020-02148-4

In the original publication, Table 1 column heads are incorrectly formatted and aligned. The corrected Table 1 is given here.

Table 1.

Clinical and molecular characteristics of ten Iberian FTLD-MAPT-P301L cases

Case Sex Age at death Duration (years) Signs at onset Initial diagnosis MAPT haplotype ApoE PMI (h) Frontal cortex Dentate nucleus of the cerebellum Hippocampus Parahippocampus
Neuronal loss/AT8 D/N Neuronal loss/AT8 D/N Neuronal loss/AT8 Neuronal loss/AT8
1 M 52 6 Behavior bvFTD H1/H1 e3/e3 13.5 ++/+++ 3.6 ± 0.2 −/− 1.0 ± 0.0 −/+++ ++/+++
2 M 58 5 Behavior bvFTD H1/H1 e3/e4 13 +++/+++ 4.1 ± 0.1 −/+ 1.0 ± 0.1 −/+++ ++/+++
8 M 58 7 Behavior bvFTD H1/H1 e3/e4 10 +++/++ 4.9 ± 0.3 −/+ 1.0 ± 0.1 −/+++ +++/+++
7a F 61 5 Behavior bvFTD H1/H1 e3/e3 14.8 ++/+++ 4.6 ± 0.1 −/+ 1.7 ± 0.1 −/+++ ++/++
4 M 72 13 Memory AD H1/H1 e3/e3 5.8 +++/+++ 3.7 ± 0.3 −/+ 1.0 ± 0.1 +/+++ +++/+++
6 M 53 7 Memory AD H1/H1 e3/e3 16.7 +++/+++ 12.6 ± 1.2 −/− 1.2 ± 0.1 −/+++ +++/+++
9 M 75 7 Behavior AD H1/H2 e3/e3 5.9 ++/+++ 5.9 ± 0.1 −/− 3.1 ± 0.1 −/+++ ++/+++
5 F 63 4 Language AD or svPPA H1/H2 e3/e3 7.3 ++/++ 4.6 ± 0.1 −/+ 1.2 ± 0.2 −/+++ ++/+++
3 M 56 10 Language svPPA H1/H1 e3/e3 6.3 +++/+++ 10.3 ± 0.9 −/+ 1.0 ± 0.1 −/+++ +++/+++
12 M 49 6 Language svPPA H1/H1 e3/e3 7.4 ++/+++ 8.2 ± 0.5 −/+ 3.3 ± 0.1 ND ND

Table after 34, arranged by initial clinical diagnosis: BvFTD behavioral variant of FTD, SvPPA semantic variant of primary progressive aphasia, AD Alzheimer disease, PMI post mortem interval. All presented cases were FUS negative, TDP43 negative. D/N denatured/native ratio in CDI assay, ± standard deviation

Age at onset was 51.3 ± 4, 60.7 ± 11.9, 50 ± 7 for bv, AD, sv respectively. Age at death was 57.3 ± 3.8, 66.7 ± 11.9 and 56 ± 7 for bv, AD, sv respectively. None of the differences in ages are significant

aAlso feature globular glial tauopathy affecting oligodendrocytes

Footnotes

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Contributor Information

Jiri G. Safar, Email: jiri.safar@case.edu

David Westaway, Email: david.westaway@ualberta.ca.


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