Assessment of D216H DYT1 polymorphism in a Chinese primary dystonia patient cohort
Author:
Publisher
Wiley
Subject
Clinical Neurology,Neurology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1468-1331.2011.03582.x/fullpdf
Reference14 articles.
1. The role of genes in causing dystonia;Schmidt;Eur J Neurol,2010
2. Intragenic cis and trans modification of genetic susceptibility in DYT1 torsion dystonia;Risch;Am J Hum Genet,2007
3. Susceptibility to DYT1 dystonia in European patients is modified by D216H polymorphism;Kamm;Neurology,2008
4. The p.Asp216His TOR1A allele effect is not found in the french population;Frederic;Mov Disord,2009
5. Effects of genetic variations in the dystonia protein torsinA: identification of polymorphism at residue 216 as protein modifier;Kock;Hum Mol Genet,2006
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1. Association of TOR1A and GCH1 Polymorphisms with Isolated Dystonia in India;Journal of Molecular Neuroscience;2020-07-13
2. Risk Factor Genes in Patients with Dystonia: A Comprehensive Review;TREMOR OTHER HYPERK;2019
3. The Role of TOR1A Polymorphisms in Dystonia: A Systematic Review and Meta-Analysis;PLOS ONE;2017-01-12
4. Lack of association between TOR1A and THAP1 mutations and sporadic adult-onset primary focal dystonia in a Chinese population;Clinical Neurology and Neurosurgery;2016-03
5. Association analysis of TOR1A polymorphisms rs2296793 and rs3842225 in a Chinese population with cervical dystonia;Neuroscience Letters;2016-01
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