Combined occurrence of deleterious TOR1A and ANO3 variants in isolated generalized dystonia
Author:
Publisher
Elsevier BV
Subject
Clinical Neurology,Geriatrics and Gerontology,Neurology
Reference5 articles.
1. Mutations in ANO3 cause dominant craniocervical dystonia: ion channel implicated in pathogenesis;G1;Am. J. Hum. Genet.,2012
2. Long-term follow-up of DYT1 dystonia patients treated by deep brain stimulation: an open-label study;Cif;Mov. Disord.,2010
3. Combined occurrence of a novel TOR1A and a THAP1 mutation in primary dystonia;Cheng;Mov. Disord.,2014
4. Epsilon-sarcoglycan mutations found in combination with other dystonia gene mutations;Klein;Ann. Neurol.,2002
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1. The Clinical Spectrum of ANO3—Report of a New Family and Literature Review;Movement Disorders Clinical Practice;2024-01-29
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