Spinocerebellar ataxia type 6 (SCA6): neurodegeneration goes beyond the known brain predilection sites-Reference-Cited by-同舟云学术

Spinocerebellar ataxia type 6 (SCA6): neurodegeneration goes beyond the known brain predilection sites

Published:2009-10 Issue:5 Volume:35 Page:515-527
ISSN:0305-1846
Container-title:Neuropathology and Applied Neurobiology
language:en
Short-container-title:

Author:

Gierga K.,Schelhaas H. J.,Brunt E. R.,Seidel K.,Scherzed W.,Egensperger R.,de Vos R. A. I.,den Dunnen W.,Ippel P. F.,Petrasch-Parwez E.,Deller T.,Schöls L.,Rüb U.

Publisher

Wiley

Subject

Physiology (medical),Clinical Neurology,Neurology,Histology,Pathology and Forensic Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2990.2009.01015.x/fullpdf

Reference58 articles.

1. Spinocerebellar ataxia type 6. Frequency of the mutation and genotype-phenotype correlations;Geschwind;Neurology,1997

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;Ishikawa;Am J Hum Genet,1997

3. Molecular features of the CAG repeats of spinocerebellar ataxia 6 (SCA6);Matsuyama;Hum Mol Genet,1997

4. SCA6 is caused by moderate CAG expansion in the alpha1A-voltage-dependent calcium channel gene;Riess;Hum Mol Genet,1997

5. Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel;Zhuchenko;Nat Genet,1997

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