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

Autor: Daude N; Centre for Prions and Protein Folding Diseases, University of Alberta, 204 Brain and Aging Research Building, Edmonton, T6G 2M8, Canada., Kim C; Department of Pathology, Case Western Reserve University, Institute of Pathology Building, Rm 406, 2085 Adelbert Road, Cleveland, OH, 44106-4907, USA., Kang SG; Centre for Prions and Protein Folding Diseases, University of Alberta, 204 Brain and Aging Research Building, Edmonton, T6G 2M8, Canada., Eskandari-Sedighi G; Centre for Prions and Protein Folding Diseases, University of Alberta, 204 Brain and Aging Research Building, Edmonton, T6G 2M8, Canada.; Department of Biochemistry, University of Alberta, Edmonton, AB, Canada., Haldiman T; Department of Pathology, Case Western Reserve University, Institute of Pathology Building, Rm 406, 2085 Adelbert Road, Cleveland, OH, 44106-4907, USA., Yang J; Centre for Prions and Protein Folding Diseases, University of Alberta, 204 Brain and Aging Research Building, Edmonton, T6G 2M8, Canada., Fleck SC; Centre for Prions and Protein Folding Diseases, University of Alberta, 204 Brain and Aging Research Building, Edmonton, T6G 2M8, Canada.; Department of Biochemistry, University of Alberta, Edmonton, AB, Canada., Gomez-Cardona E; Department of Biochemistry, University of Alberta, Edmonton, AB, Canada., Han ZZ; Centre for Prions and Protein Folding Diseases, University of Alberta, 204 Brain and Aging Research Building, Edmonton, T6G 2M8, Canada.; Department of Biochemistry, University of Alberta, Edmonton, AB, Canada., Borrego-Ecija S; Neurological Tissue Bank of the Biobanc, Hospital Clinic, IDIBAPS, Barcelona, Spain., Wohlgemuth S; Centre for Prions and Protein Folding Diseases, University of Alberta, 204 Brain and Aging Research Building, Edmonton, T6G 2M8, Canada., Julien O; Department of Biochemistry, University of Alberta, Edmonton, AB, Canada., Wille H; Centre for Prions and Protein Folding Diseases, University of Alberta, 204 Brain and Aging Research Building, Edmonton, T6G 2M8, Canada.; Department of Biochemistry, University of Alberta, Edmonton, AB, Canada., Molina-Porcel L; Neurology Department, Hospital Clinic, IDIBAPS, Barcelona, Spain., Gelpi E; Neurological Tissue Bank of the Biobanc, Hospital Clinic, IDIBAPS, Barcelona, Spain.; Division of Neuropathology and Neurochemistry, Department of Neurology, Medical University of Vienna, Vienna, Austria., Safar JG; Department of Pathology, Case Western Reserve University, Institute of Pathology Building, Rm 406, 2085 Adelbert Road, Cleveland, OH, 44106-4907, USA. jiri.safar@case.edu.; Department of Neurology, Case Western Reserve University, Institute of Pathology Building, Rm 406, 2085 Adelbert Road, Cleveland, OH, 44106-4907, USA. jiri.safar@case.edu., Westaway D; Centre for Prions and Protein Folding Diseases, University of Alberta, 204 Brain and Aging Research Building, Edmonton, T6G 2M8, Canada. david.westaway@ualberta.ca.; Department of Biochemistry, University of Alberta, Edmonton, AB, Canada. david.westaway@ualberta.ca.
Jazyk: angličtina
Zdroj: Acta neuropathologica [Acta Neuropathol] 2021 Mar; Vol. 141 (3), pp. 467-468.
DOI: 10.1007/s00401-021-02262-x
Databáze: MEDLINE