Craniocervical dystonia with levodopa-responsive parkinsonism co-segregating with a pathogenic ANO3 mutation in a Taiwanese family
Author:
Funder
Ministry of Science and Technology
National Taiwan University Hospital
Publisher
Elsevier BV
Subject
Neurology (clinical),Geriatrics and Gerontology,Neurology
Reference8 articles.
1. Mutations in ANO3 cause dominant craniocervical dystonia: ion channel implicated in pathogenesis;Charlesworth;Am. J. Hum. Genet.,2012
2. The phenotypic spectrum of DYT24 due to ANO3 mutations;Stamelou;Mov. Disord.,2014
3. Rare sequence variants in ANO3 and GNAL in a primary torsion dystonia series and controls;Zech;Mov. Disord.,2014
4. Early-onset generalized dystonia starting in the lower extremities in a patient with a novel ANO3 variant;Yoo;Park. Relat. Disord.,2018
5. A novel heterozygous ANO3 mutation with basal ganglia dysfunction in a patient with adult-onset isolated segmental dystonia;Yoo;J. Clin. Neurol.,2018
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