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Corrigendum to "Variable expressivity of KMT2B variants at codon 2565 in patients with dystonia and developmental disorders" [Parkinson. Relat. Disord. (2025) 133 107319]

Stehr, Antonia M
Author Stehr, Antonia M Institute of Human Genetics, Technical University of Munich, School of Medicine and Health, Munich, Germany
Fischer, Jan
Author Fischer, Jan Institute for Clinical Genetics, University Hospital Carl Gustav Carus at TUD Dresden University of Technology, Dresden, Germany
Mirza-Schreiber, Nazanin
Author Mirza-Schreiber, Nazanin Institute of Human Genetics, Technical University of Munich, School of Medicine and Health, Munich, Germany; Neurogenetic Systems Analysis Group, Institute of Neurogenomics, Helmholtz Munich, Neuherberg, Germany
Bernardi, Katerina
Author Bernardi, Katerina Department of Human Neurosciences, Sapienza University of Rome, Rome, Italy; Department of Pediatrics, Faculty of Medicine and University Hospital Cologne, University of Cologne, Cologne, Germany
Porrmann, Joseph
Author Porrmann, Joseph Institute for Clinical Genetics, University Hospital Carl Gustav Carus at TUD Dresden University of Technology, Dresden, Germany
Harrer, Philip
Author Harrer, Philip Institute of Human Genetics, Technical University of Munich, School of Medicine and Health, Munich, Germany; Institute of Neurogenomics, Helmholtz Zentrum München, Munich, Germany
Kaiser, Frank
Author Kaiser, Frank Institute of Human Genetics, Universitätsklinikum Essen, Essen, Germany
Jamra, Rami Abou
Author Jamra, Rami Abou Institute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany
Winkelmann, Juliane
Author Winkelmann, Juliane Institute of Human Genetics, Technical University of Munich, School of Medicine and Health, Munich, Germany; Institute of Neurogenomics, Helmholtz Zentrum München, Munich, Germany; Munich Cluster for Systems Neurology (SyNergy), Munich, Germany; DZPG, Deutsches Zentrum für Psychische Gesundheit, Munich, Germany
Jech, Robert
Author Jech, Robert Department of Neurology, Charles University, 1st Faculty of Medicine and General University Hospital in Prague, Prague, Czech Republic
Koy, Anne
Author Koy, Anne Department of Pediatrics, Faculty of Medicine and University Hospital Cologne, University of Cologne, Cologne, Germany; Center for Rare Diseases, Faculty of Medicine and University Hospital Cologne, University of Cologne, Cologne, Germany
Oexle, Konrad
Author Oexle, Konrad Institute of Human Genetics, Technical University of Munich, School of Medicine and Health, Munich, Germany; Neurogenetic Systems Analysis Group, Institute of Neurogenomics, Helmholtz Munich, Neuherberg, Germany; Institute of Neurogenomics, Helmholtz Zentrum München, Munich, Germany
Zech, Michael
Author Zech, Michael Institute of Human Genetics, Technical University of Munich, School of Medicine and Health, Munich, Germany; Institute of Neurogenomics, Helmholtz Zentrum München, Munich, Germany; Institute for Advanced Study, Technical University of Munich, Garching, Germany. Electronic address: michael.zech@mri.tum.de

Parkinsonism & related disorders. 2025 May ; 134 () : 107795. [epub] 20250323

Parkinsonism Relat Disord
ISSN 1873-5126 | 1353-8020
Source

Status PubMed-not-MEDLINE Language English Country England, Great Britain Media print-electronic

Document type Published Erratum

Persistent link https://www.medvik.cz/link/pmid40120210

PubMed 40120210
DOI 10.1016/j.parkreldis.2025.107795
PII: S1353-8020(25)00536-X
Knihovny.cz E-resources

Publication type
Published Erratum MeSH

Department of Human Neurosciences Sapienza University of Rome Rome Italy; Department of Pediatrics Faculty of Medicine and University Hospital Cologne University of Cologne Cologne Germany

Department of Neurology Charles University 1st Faculty of Medicine and General University Hospital Prague Prague Czech Republic

Department of Pediatrics Faculty of Medicine and University Hospital Cologne University of Cologne Cologne Germany; Center for Rare Diseases Faculty of Medicine and University Hospital Cologne University of Cologne Cologne Germany

Institute for Clinical Genetics University Hospital Carl Gustav Carus at TUD Dresden University of Technology Dresden Germany

Institute of Human Genetics Technical University of Munich School of Medicine and Health Munich Germany

Institute of Human Genetics Technical University of Munich School of Medicine and Health Munich Germany; Institute of Neurogenomics Helmholtz Zentrum München Munich Germany

Institute of Human Genetics Technical University of Munich School of Medicine and Health Munich Germany; Institute of Neurogenomics Helmholtz Zentrum München Munich Germany; Institute for Advanced Study Technical University of Munich Garching Germany

Institute of Human Genetics Technical University of Munich School of Medicine and Health Munich Germany; Institute of Neurogenomics Helmholtz Zentrum München Munich Germany; Munich Cluster for Systems Neurology Munich Germany; DZPG Deutsches Zentrum für Psychische Gesundheit Munich Germany

Institute of Human Genetics Technical University of Munich School of Medicine and Health Munich Germany; Neurogenetic Systems Analysis Group Institute of Neurogenomics Helmholtz Munich Neuherberg Germany

Institute of Human Genetics Universitätsklinikum Essen Essen Germany

Institute of Human Genetics University of Leipzig Medical Center Leipzig Germany

Erratum For

Parkinsonism Relat Disord. 2025 Apr;133:107319. doi: 10.1016/j.parkreldis.2025.107319. PubMed

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Corrigendum to "Variable expressivity of KMT2B variants at codon 2565 in patients with dystonia and developmental disorders" [Parkinson. Relat. Disord. (2025) 133 107319]

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