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DYT-TOR1A dystonia: an update on pathogenesis and treatment

DYT-TOR1A dystonia is a neurological disorder characterized by involuntary muscle contractions and abnormal movements. It is a severe genetic form of dystonia caused by mutations in the TOR1A gene. TorsinA is a member of the AAA + family of adenosine triphosphatases (ATPases) involved in a variety o...

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Detalles Bibliográficos
Autores principales: Fan, Yuhang, Si, Zhibo, Wang, Linlin, Zhang, Lei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10448058/
https://www.ncbi.nlm.nih.gov/pubmed/37638318
http://dx.doi.org/10.3389/fnins.2023.1216929