Spinocerebellar ataxia type 6 (SCA6): Clinical pilot trial with gabapentin

Author:

Nakamura Katsuya,Yoshida Kunihiro,Miyazaki Daigo,Morita Hiroshi,Ikeda Shu-ichi

Publisher

Elsevier BV

Subject

Clinical Neurology,Neurology

Reference21 articles.

1. Bird TD. Hereditary ataxia overview. In: Gene Reviews: Genetic Disease Online Reviews at GeneTest-GeneClinics[database online].[cited 28 February 2008]. Copyright, University of Washington, Seattle, Available at http://www.geneclinics.org/.

2. Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis;Schöls;Lancet Neurol,2004

3. Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the α1A-voltage-dependent calcium channel;Zhuchenko;Nat Genet,1997

4. SCA6 is caused by moderate CAG expansion in the α1A-voltage-dependent calcium channel gene;Riess;Hum Mol Genet,1997

5. The hereditary spinocerebellar ataxias in Japan;Sasaki;Cytogenet Genome Res,2003

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