Severe and rapidly progressing cognitive phenotype in a SCA17-family with only marginally expanded CAG/CAA repeats in the TATA-box binding protein gene: A case report

Overview of attention for article published in BMC Neurology, August 2012

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Background: The autosomal dominant spinocerebellar ataxias (SCAs) confine a group of rare and heterogeneous disorders http://t.co/3MupXIXb

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#neurology twts: Severe and rapidly progressing cognitive phenotype in a SCA17-family with only marginally expan... http://t.co/JMRZ6uED

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