Homozygous Pathogenic MYH3 Variants Associated With Arthrogryposis and Lingual Dystonia
Authors
Charlotte Mouraux
GIGA – CRC Human Imaging – Rare Movement Disorders Research Group, University of Liège, Liège; Department of Human Genetics, University Hospital of Liège, Liège
Claire Fouquet
Department of Human Genetics, University Hospital of Liège, Liège
Keith Durkin
Department of Human Genetics, University Hospital of Liège, Liège; Laboratory of Human Genetics, GIGA-Institute, University of Liège, Liège
Vinciane Dideberg
Department of Human Genetics, University Hospital of Liège, Liège
David Aktan
GIGA – CRC Human Imaging – Rare Movement Disorders Research Group, University of Liège, Liège; Department of Neurology, University Hospital of Liège, Liège
Maria Artesi
GIGA – CRC Human Imaging – Rare Movement Disorders Research Group, University of Liège, Liège; Department of Human Genetics, University Hospital of Liège, Liège; Laboratory of Human Genetics, GIGA-Institute, University of Liège, Liège
Frédérique Depierreux
frederique.depierreux@chuliege.be
GIGA – CRC Human Imaging – Rare Movement Disorders Research Group, University of Liège, Liège; Department of Neurology, University Hospital of Liège, Liège
DOI: https://doi.org/10.5334/tohm.1079 | Journal eISSN: 2160-8288
Language: English
Submitted on: Jul 17, 2025
Accepted on: Oct 16, 2025
Published on: Oct 27, 2025
Published by: Ubiquity Press
In partnership with: Paradigm Publishing Services
Publication frequency: 1 issue per year
Keywords:
© 2025 Charlotte Mouraux, Claire Fouquet, Keith Durkin, Vinciane Dideberg, Saskia Bulk, David Aktan, Maria Artesi, Frédérique Depierreux, published by Ubiquity Press
This work is licensed under the Creative Commons Attribution 4.0 License.