The molecular basis of spinocerebellar ataxia type 48 caused by a de novo mutation in the ubiquitin ligase CHIP
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Title
The molecular basis of spinocerebellar ataxia type 48 caused by a de novo mutation in the ubiquitin ligase CHIP
Authors
Keywords
ataxia, E3 ubiquitin ligase, chaperone, neurodegeneration, neurodegenerative disease
Journal
JOURNAL OF BIOLOGICAL CHEMISTRY
Volume 298, Issue 5, Pages 101899
Publisher
Elsevier BV
Online
2022-04-07
DOI
10.1016/j.jbc.2022.101899
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