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...
Main Authors: | Richard J Burman, Lauren M Watson, Danielle C Smith, Joseph V Raimondo, Robea Ballo, Janine Scholefield, Sally A Cowley, Matthew J A Wood, Susan H Kidson, Leslie J Greenberg |
---|---|
Format: | Article |
Language: | English |
Published: |
Public Library of Science (PLoS)
2021-01-01
|
Series: | PLoS ONE |
Online Access: | https://doi.org/10.1371/journal.pone.0247434 |
Similar Items
-
Molecular and electrophysiological features of spinocerebellar ataxia type seven in induced pluripotent stem cells.
by: Burman, RJ, et al.
Published: (2021) -
Spinocerebellar ataxia type 7 in South Africa: epidemiology, pathogenesis and therapy
by: Watson, L, et al.
Published: (2016) -
Spinocerebellar Ataxias
by: Huda Y. Zoghbi
Published: (2000-10-01) -
Spinocerebellar ataxias Ataxias espinocerebelares
by: Hélio A.G. Teive
Published: (2009-12-01) -
Postural Tremor and Ataxia Progression in Spinocerebellar Ataxias
by: Shi-Rui Gan, et al.
Published: (2017-10-01)