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Showing articles 0 to 4 of 4 Filter Applied: cerebellar atrophy,primary (Click to remove) SPG7 Mutations Explain a Significant Proportion of French Canadian Spastic Ataxia Cases Eur J Hum Genet 24:1016-1021, Choquet,K.,et al, 2016 The Autosomal Recessive Cerebellar Ataxias NEJM 366:636-646, Anheim,M.,et al, 2012 A 23-Year-Old Man With Seizures and Visual Deficit Neurol 70:73-78, Boustany,R.-M.,et al, 2008 Gerstmann-Straussler-Scheinker Disease, I, Extending the Clinical Spectrum Neurol 39:1446-1452, Farlow,M.R.,et al, 1989 Showing articles 0 to 4 of 4