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MR Imaging of SCA3/MJD

Spinocerebellar ataxia type 3/Machado–Joseph disease (SCA3/MJD) is a progressive autosomal dominantly inherited cerebellar ataxia characterized by the aggregation of polyglutamine-expanded protein within neuronal nuclei in the brain, which can lead to brain damage that precedes the onset of clinical...

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Detalles Bibliográficos
Autores principales: Wan, Na, Chen, Zhao, Wan, Linlin, Tang, Beisha, Jiang, Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7417615/
https://www.ncbi.nlm.nih.gov/pubmed/32848545
http://dx.doi.org/10.3389/fnins.2020.00749