Behavioral disorder, dementia, ataxia, and rigidity in a large family with TATA box-binding protein mutation
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Autosomal dominant cerebellar ataxia type I. Nerve conduction and evoked potential studies in families with SCA1, SCA2 and SCA3
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Autosomal dominant cerebellar ataxia type I: Multimodal electrophysiological study and comparison between SCA1 and SCA2 patients
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Clinical features and neuropathology of autosomal dominant spinocerebellar ataxia (SCA17)
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Neural generators of tibial nerve P30 somatosensory evoked potential studied in patients with a focal lesion of the cervicomedullary junction
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CAG repeat expansion in the TATA box-binding protein gene causes autosomal dominant cerebellar ataxia
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