Unusual phenotypes in DYT1 dystonia: A report of five cases and a review of the literature
Author:
Publisher
Wiley
Subject
Clinical Neurology,Neurology
Reference22 articles.
1. Dystonia in Ashkenazi Jews: clinical characterisation of a founder mutation;Bressman;Ann Neurol,1994
2. The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein;Ozelius;Nat Genet,1997
3. The DYT1 phenotype and guidelines for diagnostic testing;Bressman;Neurology,2000
4. A common 3-bp deletion in the DYT1 gene in Russian families with early-onset torsion dystonia;Slominsky;Hum Mutat,1999
5. The role of DYT1 in primary torsion dystonia in Europe;Valente;Brain,1998
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