Exome sequencing reveals a novel TTC19 mutation in an autosomal recessive spinocerebellar ataxia patient (Q35084390)

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

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