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Showing articles 0 to 4 of 4 Filter Applied: cerebellar ataxia,hereditary (Click to remove) The Expansion of the CAG Repeat in Ataxin-2 is a Frequent Cause of Autosomal Dominant Spinocerebellar Ataxia Neurol 49:1009-1013, Lorenzetti,D.,et al, 1997 Spinocerebellar Ataxia Type 6, Molecular & Clin Features of 35 Japanese Pts (1 Homozygous for CAG Repeat Expan) Neurol 49:1238-1243, 11961997., Matsumura,R.,et al, 1997 Clinical, Neuropath & Genetic Studies of Large Spinocerebellar Ataxia Type 1 (SCA1) Kindred: (CAG) n Early Premonitory Signs & Symp Neurol 45:24-30, Genis,D.,et al, 1995 Autosomal Dominant Cerebellar Phenotypes:The Genotype has Settled the Issue Neurol 45:1-5, Rosenberg,R.N., 1995 Showing articles 0 to 4 of 4