Twelve‐year Follow‐up of A Large Italian Family with Atypical Phenotypes of DYT1‐dystonia
Author:
Affiliation:
1. Department of Neurosciences, Biomedicine and Movement Sciences, Section of NeurologyUniversity of Verona Verona Italy
2. Physical Medicine and Rehabilitation UnitAzienda ULSS 9 Scaligera Verona Italy
Publisher
Wiley
Subject
Neurology (clinical),Neurology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/mdc3.12712
Reference10 articles.
1. The DYT1 phenotype and guidelines for diagnostic testing
2. Diagnostic criteria for dystonia in DYT1 families
3. The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein
4. Phenotypic expression of the DYT1 mutation: A family with writer's cramp of juvenile onset
5. Phenotypic variability of the DYT1 mutation in German dystonia patients
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