Molecular and electrophysiological features of spinocerebellar ataxia type seven in induced pluripotent stem cells

Spinocerebellar ataxia type 7 (SCA7) is an inherited neurodegenerative disease caused by a polyglutamine repeat expansion in the ATXN7 gene. Patients with this disease suffer from a degeneration of their cerebellar Purkinje neurons and retinal photoreceptors that result in a progressive ataxia and l...

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Detalhes bibliográficos
Publicado no:PLoS One
Main Authors: Burman, Richard J., Watson, Lauren M., Smith, Danielle C., Raimondo, Joseph V., Ballo, Robea, Scholefield, Janine, Cowley, Sally A., Wood, Matthew J. A., Kidson, Susan H., Greenberg, Leslie J.
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2021
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7904216/
https://ncbi.nlm.nih.gov/pubmed/33626063
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0247434
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