Article info
PDFNeurogenetics
Original research
Dissecting genetic architecture of rare dystonia: genetic, molecular and clinical insights
- Correspondence to Dr Ebba Lohmann, Eberhard Karls Universitat Tubingen Hertie Institut fur klinische Hirnforschung Allgemeine Neurologie, Tübingen 72076, Germany; ebbalohmann{at}gmx.net
Citation
Dissecting genetic architecture of rare dystonia: genetic, molecular and clinical insights
Publication history
- Received December 8, 2022
- Accepted December 24, 2023
- First published March 8, 2024.
Online issue publication
April 19, 2024
Article Versions
- Previous version (8 March 2024).
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Supplementary Data
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© Author(s) (or their employer(s)) 2024. Re-use permitted under CC BY. Published by BMJ. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution 4.0 Unported (CC BY 4.0) license, which permits others to copy, redistribute, remix, transform and build upon this work for any purpose, provided the original work is properly cited, a link to the licence is given, and indication of whether changes were made. See: https://creativecommons.org/licenses/by/4.0/.