Targeted gene capture sequencing in diagnosis of dystonia patients
Author:
Funder
Natural Science Foundation of China
Publisher
Elsevier BV
Subject
Neurology (clinical),Neurology
Reference27 articles.
1. Phenomenology and classification of dystonia: a consensus update;Albanese;Mov. Disord.,2013
2. Update on the genetics of dystonia;Lohmann;Curr. Neurol. Neurosci. Rep.,2017
3. Special concerns in defining, studying, and treating dystonia in children;Mink;Mov. Disord.,2013
4. Primary dystonias and genetic disorders with dystonia as clinical feature of the disease;Moghimi;Eur. J. Paediatr. Neurol.,2014
5. Genetics of movement disorders in the next-generation sequencing era;Olgiati;Mov. Disord.,2016
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1. Genome sequencing reanalysis increases the diagnostic yield in dystonia;Parkinsonism & Related Disorders;2024-07
2. Dissecting genetic architecture of rare dystonia: genetic, molecular and clinical insights;Journal of Medical Genetics;2024-03-08
3. Clinical and genetic profile of patients with dystonia: An experience from a tertiary neurology center from India;Parkinsonism & Related Disorders;2024-03
4. The Clinical Spectrum of ANO3—Report of a New Family and Literature Review;Movement Disorders Clinical Practice;2024-01-29
5. Genetic spectrum and clinical features in a cohort of Chinese patients with isolated dystonia;Clinical Genetics;2023-01-24
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