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April 22, 2003Brain

Huntington's disease-like phenotype due to trinucleotide repeat expansions in the TBP and JPH3 genes

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Authors

GSGiovanni StévaninCentre Hospitalier Universitaire de Bordeaux

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Giovanni Stévanin (2003) studied this question.

synapsesocial.com/papers/6aae314d9e60580df61647aahttps://doi.org/10.1093/brain/awg155
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Also Consider

Synapse has enriched 4 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1CAG repeat expansion in the TATA box-binding protein gene causes autosomal dominant cerebellar ataxia2001 · 164 citations
  2. 2A disorder similar to Huntington's disease is associated with a novel CAG repeat expansion2001 · 167 citations
  3. 3A neurological disease caused by an expanded CAG trinucleotide repeat in the TATA-binding protein gene: a new polyglutamine disease? [In Process Citation]1999 · 398 citations
  4. 4CAG/CTG repeat expansions at the Huntington’s disease–like 2 locus are rare in Huntington’s disease patients2002 · 55 citations