A knockin mouse model of spinocerebellar ataxia type 3 exhibits prominent aggregate pathology and aberrant splicing of the disease gene transcript
Work
Year: 2014
Type: article
Abstract: Polyglutamine diseases, including spinocerebellar ataxia type 3 (SCA3), are caused by CAG repeat expansions that encode abnormally long glutamine repeats in the respective disease proteins. While the ... more
Source: Human Molecular Genetics
Authors Biswarathan Ramani, Ginny Marie Harris, Rogerio Huang, Takahiro Seki, Geoffrey G. Murphy +6 more
Institutions University of Iowa, Laboratoire d’immunologie intégrative du cancer, University of Florida, University of Michigan
Cites: 70
Cited by: 45
Related to: 10
FWCI: 1.226
Citation percentile (by year/subfield): 77.77
Subfield: Cellular and Molecular Neuroscience
Field: Neuroscience
Domain: Life Sciences
Open Access status: bronze
Grant IDS RO1NS038712, F31NS083167, RO3NS072967