On autosomal dominant cerebellar ataxia (ADCA) other than polyglutamine diseases, with special reference to chromosome 16q22.1-linked ADCA
Author:
Publisher
Wiley
Subject
Neurology (clinical),General Medicine,Pathology and Forensic Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1440-1789.2006.00719.x/fullpdf
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2. Japanese Families with Autosomal Dominant Pure Cerebellar Ataxia Map to Chromosome 19p13.1-p13.2 and Are Strongly Associated with Mild CAG Expansions in the Spinocerebellar Ataxia Type 6 Gene in Chromosome 19p13.1
3. 3. DI Graham, and PL Lantos , eds., 7th edn , Vol. 2 . London: Arnold, 2002 .
4. Protein aggregation and neurodegenerative disease
5. An untranslated CTG expansion causes a novel form of spinocerebellar ataxia (SCA8)
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