Spinocerebellar ataxia 8: Variable phenotype and unique pathogenesis
Author:
Publisher
Elsevier BV
Subject
Clinical Neurology,Geriatrics and Gerontology,Neurology
Reference48 articles.
1. An untranslated CTG expansion causes a novel form of spinocerebellar ataxia (SCA8);Koob;Nat Genet,1999
2. Molecular genetics of spinocerebellar ataxia type 8 (SCA8);Mutsuddi;RNA Biol,2005
3. If it's not one thing, it's another;Paulson;Nat Genet,2006
4. Bidirectional expression of CUG and CAG expansion transcripts and intranuclear polyglutamine inclusions in spinocerebellar ataxia type 8;Moseley;Nat Genet,2006
5. SCA8 BAC transgenic mice have a progressive and lethal neurological phenotype demonstrating pathogenicity of the CTG expansion;Moseley;Am J Hum Genet,2002
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