Mutant ataxin1 disrupts cerebellar development in spinocerebellar ataxia type 1
Author:
Funder
Northwestern University
Publisher
American Society for Clinical Investigation
Subject
General Medicine
Link
https://www.jci.org/articles/view/96765/files/pdf
Reference59 articles.
1. Identification and characterization of the gene causing type 1 spinocerebellar ataxia
2. A Cellular System that Degrades Misfolded Proteins and Protects against Neurodegeneration
3. Expression analysis of the ataxin–1 protein in tissues from normal and spinocerebellar ataxia type 1 individuals
4. A Long CAG Repeat in the Mouse Sca1 Locus Replicates SCA1 Features and Reveals the Impact of Protein Solubility on Selective Neurodegeneration
5. Brain pathology of spinocerebellar ataxias
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