Two Cases of Spinocerebellar Ataxia Accompanied by Involvement of the Skeletal Motor Neuron System and Bulbar Palsy
Author:
Affiliation:
1. Department of Neurology, Graduate School of Medicine, Dentistry and Pharmacy, Okayama University
Publisher
Japanese Society of Internal Medicine
Subject
General Medicine,Internal Medicine
Link
http://www.jstage.jst.go.jp/article/internalmedicine/46/11/46_11_751/_pdf
Reference20 articles.
1. Analysis of spinocerebellar ataxia type 1 (SCA1)-related CAG trinucleotide expansion in Japan
2. Molecular and Clinical Correlations in Spinocerebellar Ataxia 2: A Study of 32 Families
3. Phenotype variation correlates with CAG repeat length in SCA2 - A study of 28 Japanese patients
4. Machado-Joseph disease: An autosomal dominant motor system degeneration
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