Membrane defects and genetic redundancy: Are we at a turning point for DYT1 dystonia?
Author:
Affiliation:
1. Vlaams Instituut voor Biotechnologie Centre for the Biology of DiseaseLeuven Belgium
2. KU Leuven, Department of Human GeneticsLeuven Belgium
Funder
Vlaams Instituut voor Biotechnologie
Publisher
Wiley
Subject
Clinical Neurology,Neurology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/mds.26880
Reference109 articles.
1. The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein
2. Phenomenology and classification of dystonia: A consensus update
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4. Genetic and clinical features of primary torsion dystonia
5. Primary dystonia and dystonia-plus syndromes: clinical characteristics, diagnosis, and pathogenesis
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