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    Analysis of spinocerebellar ataxia types 1, 2, 3, and 6, dentatorubral-pallidoluysian atrophy, and Friedreich's ataxia genes in spinocerebellar ataxia patients in the UK 

    Leggo J.; Dalton A.; Morrison P.J.; Dodge A.; Connarty M.; Kotze M.J.; Rubinsztein D.C. (1997)
    Accurate clinical diagnosis of the spino-cerebellar ataxias (SCAs) can be diffcult because of overlap in phenotype with other disorders and variation in clinical manifestations. Six SCA loci have been mapped and four disease ...

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    AuthorConnarty M. (1)Dalton A. (1)
    Dodge A. (1)
    Kotze M.J. (1)Leggo J. (1)Morrison P.J. (1)Rubinsztein D.C. (1)SubjectAdolescent (1)Adult (1)africa (1)Aged (1)aged (1)allele (1)
    article (1)
    autosomal dominant disorder (1)Calcium Channels (1)cerebellar ataxia (1)... View MoreDate Issued
    1997 (1)
    Has File(s)
    No (1)
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