1. Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1;Orr;Nat Genet,1993
2. Analysis of spinocerebellar ataxia types 1,2,3 and 6, dentatorubral-pallidoluysian atrophy and Friedreich's ataxia genes in a group of spinocerebellar ataxia patients in the United Kingdom;Leggo;J Med Genet,1997
3. The prevalence and wide clinical spectrum of the spinocerebellar ataxia type 2 trinucleotide repeat in patients with autosomal dominant cerebellar ataxia;Geschwind;Am J Hum Genet,1997
4. Marked phenotypic heterogeneity associated with expansion of a CAG repeat sequence at the spinocerebellar ataxia 3/Machado Joseph disease locus;Cancel;Am J Hum Genet,1996
5. Autosomal dominant spinocerebellar ataxia with sensory axonal neuropathy (SCA4): clinical description and genetic localisation to chromosome 16q22.1;Flanigan;Am J Hum Genet,1996