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Záznam pochází z PubMed

Correction to: Myoclonic dystonia phenotype related to a novel calmodulin-binding transcription activator 1 sequence variant

Dzinovic, Ivana
Autor Dzinovic, Ivana Institute of Neurogenomics, Helmholtz Zentrum München, Munich, Germany
Serranová, Tereza
Autor Serranová, Tereza Department of Neurology, 1st Faculty of Medicine and General University Hospital in Prague, Charles University, Prague, Czech Republic
Prouteau, Clement
Autor Prouteau, Clement Department of Biochemistry and Genetics, University Hospital Angers, Angers, France
Colin, Estelle
Autor Colin, Estelle Department of Biochemistry and Genetics, University Hospital Angers, Angers, France
Ziegler, Alban
Autor Ziegler, Alban Department of Biochemistry and Genetics, University Hospital Angers, Angers, France
Winkelmann, Juliane
Autor Winkelmann, Juliane Institute of Neurogenomics, Helmholtz Zentrum München, Munich, Germany Institute of Human Genetics, Technical University of Munich, Munich, Germany Lehrstuhl Für Neurogenetik, Technische Universität München, Munich, Germany Munich Cluster for Systems Neurology, SyNergy, Munich, Germany
Jech, Robert
Autor Jech, Robert Department of Neurology, 1st Faculty of Medicine and General University Hospital in Prague, Charles University, Prague, Czech Republic. jech@cesnet.cz
Zech, Michael
Autor Zech, Michael ORCID Institute of Neurogenomics, Helmholtz Zentrum München, Munich, Germany. michael.zech@helmholtz-muenchen.de Institute of Human Genetics, Technical University of Munich, Munich, Germany. michael.zech@helmholtz-muenchen.de

Neurogenetics. 2022 Jan ; 23 (1) : 77.

ISSN 1364-6753 | 1364-6745
Zdroj

Status PubMed-not-MEDLINE Jazyk angličtina Země Spojené státy americké Médium print

Typ dokumentu tisková chyba

Perzistentní odkaz https://www.medvik.cz/link/pmid34859314

PubMed 34859314
DOI 10.1007/s10048-021-00641-w
PII: 10.1007/s10048-021-00641-w
Knihovny.cz E-zdroje

Publikační typ
tisková chyba MeSH

Department of Biochemistry and Genetics University Hospital Angers Angers France

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

Institute of Human Genetics Technical University of Munich Munich Germany

Institute of Neurogenomics Helmholtz Zentrum München Munich Germany

Lehrstuhl Für Neurogenetik Technische Universität München Munich Germany

Munich Cluster for Systems Neurology SyNergy Munich Germany

Erratum pro

Neurogenetics. 2021 May;22(2):137-141. doi: 10.1007/s10048-021-00637-6. PubMed

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