ANO3 Mutations in Chinese Dystonia: A Genetic Screening Study Using Next-Generation Sequencing
Author:
Publisher
Frontiers Media SA
Subject
Clinical Neurology,Neurology
Reference14 articles.
1. Phenomenology and classification of dystonia: a consensus update;Albanese;Mov Disord.,2013
2. Mutations in ANO3 cause dominant craniocervical dystonia: ion channel implicated in pathogenesis;Charlesworth;Am J Hum Genet,2012
3. Rare sequence variants in ANO3 and GNAL in a primary torsion dystonia series and controls;Zech;Mov Disord,2014
4. Mutations in ANO3 and GNAL gene in thirty-three isolated dystonia families;Ma;Mov Disord.,2015
5. The phenotypic spectrum of DYT24 due to ANO3 mutations;Stamelou;Mov Disord,2014
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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
2. Broadening the clinical spectrum: molecular mechanisms and new phenotypes of ANO3-dystonia;Brain;2023-12-11
3. Generalized Dystonia With Tremor and Myoclonus Associated With ANO3 Variant;Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques;2023-08-29
4. A novel ANO3 variant in two siblings with different phenotypes;Parkinsonism & Related Disorders;2023-06
5. A novel variant in the transmembrane 4 domain of ANO3 identified in a two-year-old girl with developmental delay and tremor;Journal of Human Genetics;2022-09-27
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