Clinical Features,DYT1Mutation Screening and Genotype-Phenotype Correlation in Patients with Dystonia from Iran
Author:
Publisher
S. Karger AG
Subject
General Medicine
Reference28 articles.
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2. The AAA+ protein torsinA interacts with a conserved domain present in LAP1 and a novel ER protein
3. The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein
4. A systematic review on the diagnosis and treatment of primary (idiopathic) dystonia and dystonia plus syndromes: report of an EFNS/MDS-ES Task Force
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1. Investigating DYT1 in a Taiwanese dystonia cohort;Journal of the Formosan Medical Association;2022-01
2. TorsinA restoration in a mouse model identifies a critical therapeutic window for DYT1 dystonia;Journal of Clinical Investigation;2021-03-15
3. TorsinB overexpression prevents abnormal twisting in DYT1 dystonia mouse models;eLife;2020-03-23
4. TorsinB overexpression prevents abnormal twisting in DYT1 dystonia mouse models;2019-11-11
5. Primary generalized dystonia due to TOR1A ΔGAG mutation in an Indian family with intrafamilial clinical heterogeneity;Neurology India;2019
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