6 results on '"Sweeney, Mary G."'
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2. An ITPR1 gene deletion causes spinocerebellar ataxia 15/16: A genetic, clinical and radiological description
3. Huntingtonʼs disease phenocopies are clinically and genetically heterogeneous
4. Spinocerebellar ataxia type 17: Extension of phenotype with putaminal rim hyperintensity on magnetic resonance imaging
5. Parkinsonism and Nigrostriatal Dysfunction Are Associated With Spinocerebellar Ataxia Type 6 (Sca6)
6. Generalized chorea in two patients harboring the Friedreich's ataxia gene trinucleotide repeat expansion
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