Exome sequencing reveals a novel TTC19 mutation in an autosomal recessive spinocerebellar ataxia patient

Overview of attention for article published in BMC Neurology, January 2014

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Exome sequencing reveals a novel TTC19 mutation in an autosomal recessive spinocerebellar ataxia patient. http://t.co/3FhNo0Tm6y

Exome sequencing reveals a novel TTC19 mutation in an autosomal recessive spinocerebellar ataxia patient. http://t.co/CbvdeoWl3E

Exome sequencing reveals a novel TTC19 mutation in an autosomal recessive spinocerebellar ataxia patient. http://t.co/pzdmsYmRjQ

#neurology Exome sequencing reveals a novel TTC19 mutation in an autosomal recessive spinocerebellar ataxia pa... http://t.co/Gjs28WbxXD

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