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

Dzinovic, Ivana; Serranová, Tereza; Prouteau, Clement; Colin, Estelle; Ziegler, Alban; Winkelmann, Juliane; Jech, Robert; Zech, Michael

Dzinovic, Ivana; Serranová, Tereza; Prouteau, Clement; Colin, Estelle; Ziegler, Alban; Winkelmann, Juliane; Jech, Robert; Zech, Michael.

Afiliação

Dzinovic I; Institute of Neurogenomics, Helmholtz Zentrum München, Munich, Germany.
Serranová T; Department of Neurology, 1st Faculty of Medicine and General University Hospital in Prague, Charles University, Prague, Czech Republic.
Prouteau C; Department of Biochemistry and Genetics, University Hospital Angers, Angers, France.
Colin E; Department of Biochemistry and Genetics, University Hospital Angers, Angers, France.
Ziegler A; Department of Biochemistry and Genetics, University Hospital Angers, Angers, France.
Winkelmann J; Institute of Neurogenomics, Helmholtz Zentrum München, Munich, Germany.
Jech R; Institute of Human Genetics, Technical University of Munich, Munich, Germany.
Zech M; Lehrstuhl Für Neurogenetik, Technische Universität München, Munich, Germany.

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

Article em En | MEDLINE | ID: mdl-34859314

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Neurogenetics Assunto da revista: GENETICA / NEUROLOGIA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Alemanha

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