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1. Nuclear inclusions in spinocerebellar ataxia type 1

2. Clinical and genetic analysis of three German kindreds with autosomal dominant cerebellar ataxia type I linked to the SCA2locus

3. Fourth meeting of the European Neurological Society 25–29 June 1994 Barcelona, Spain

4. The gene for autosomal dominant cerebellar ataxia with pigmentary macular dystrophy maps to chromosome 3p12–p21.1

5. The gene for Machado–Joseph disease maps to the same 3-cM interval as the spinal cerebellar ataxia 3 gene on chromosome 14q

6. Clinical and genetic analysis of a Tunisian family with autosomal dominant cerebellar ataxia type 1linked to the SCA2 locus

7. Clinical and molecular features of spinocerebellar ataxia type 6

8. Linkage disequilibrium at the SCA2 locus

10. Phenotypic variability in autosomal dominant cerebellar ataxia type I is unrelated to genetic heterogeneity

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