| Document Date: 2015-04-17 06:57:28
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City New York / / Continent Europe / / Country Japan / India / / / Facility Zoology University of Mysore / Thangaraj K. Complex / / IndustryTerm therapy for polyglutamine neurodegenerative diseases / food habits / / MedicalCondition ataxia / common complex genetic disorders / autosomal dominant cerebellar ataxia / cerebellar degenerative disorders / autosomal dominant spinocerebellar ataxias / polyglutamine neurodegenerative diseases / dominant cerebellar ataxias / Riess O. Autosomal dominant cerebellar ataxias / disease / toxic gainof-function disease / dominant spinocerebellar ataxias / dentatorubral-pallidoluysian atrophy / only autosomal dominant ataxia / spinocerebellar ataxia suppression / retinal degeneration / Spinocerebellar ataxias / rare complex disorders / Sporadic ataxias / progressive ataxia / autosomal dominant ataxias - SCA1 / Spinocerebellar ataxia type / disorder / polyglutamine diseases / Neurodegenerative diseases / MS / polyQ disorders / Spinocerebellar ataxia 7 / hereditary neurodegenerative disorders / generalized incoordination / gait ataxia / Ataxic Diseases / disorders / genetic disorders / Sanchez I. the spinocerebellar ataxias / / Organization Kusuma L. Genetics and Genomics Laboratory Department of Studies / University of Mysore / / Person Gene Seq / / Position Libby RT / editor / / ProvinceOrState Karnataka / Georgia / / PublishedMedium PLoS One / / Region Central Asia / Middle East / / Technology Genomics / gene expression / /
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Indian J Med Res 141, February 2015, ppCommentary An understanding of spinocerebellar ataxia Advances in molecular genetics techniques have