ANO3 Mutations in Chinese Dystonia: A Genetic Screening Study Using Next-Generation Sequencing
Background: Dystonia-24 (DYT24) is a monogenic autosomal dominant dystonia caused by mutations in the gene ANO3, which has shown phenotypic and genotypic heterogeneity according to previous reports.Objective: To screen and identify ANO3 mutations in a cohort of patients with dystonia in China and to...
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| Principais autores: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Frontiers Media S.A.
2020-02-01
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| coleção: | Frontiers in Neurology |
| Assuntos: | |
| Acesso em linha: | https://www.frontiersin.org/article/10.3389/fneur.2019.01351/full |
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