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Authors
Thieme, Andreas https://orcid.org/0000-0001-6221-8601
Faber, Jennifer
Sulzer, Patricia
Reetz, Kathrin
Dogan, Imis
Barkhoff, Miriam
Krahe, Janna
Jacobi, Heike
Aktories, Julia-Elisabeth
Minnerop, Martina
Elben, Saskia
van der Veen, Raquel
Müller, Johanna
Batsikadze, Giorgi
Konczak, Jürgen
Synofzik, Matthis
Roeske, Sandra
Timmann, Dagmar
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Funding
Funding for this research was provided by:
Deutsche Forschungsgemeinschaft (FU356/12-1)
Deutsche Forschungsgemeinschaft (441409627)
European Joint Programme on Rare Diseases (825575)
German Heredoataxia Societey (-)
Freunde and Förderer der Neurologie am Universitätsklinikum Essen (-)
Universität Duisburg-Essen
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Article History
Received: 11 November 2021
Revised: 22 February 2022
Accepted: 23 February 2022
First Online: 1 April 2022
Declarations
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: All authors declare no financial disclosures or conflicts of interest other than the funding stated below concerning the research covered in this manuscript.
: The study has prospectively been registered at the German Clinical Study Register (; DRKS-ID: DRKS00016854).
: This study was approved by the local ethics committees of the participating sites and performed in accordance with the ethical standards laid down in the Declaration of Helsinki of 1964 and its later amendments.
: Participants’ consent was obtained prior to any study related procedures.
