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March 4, 2003BrainOpen Access

Homozygosity for CAG mutation in Huntington disease is associated with a more severe clinical course

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Authors

FSFerdinando SquitieriCasa Sollievo della Sofferenza

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Cite This Study

Ferdinando Squitieri (2003) studied this question.

synapsesocial.com/papers/6a01488dda5c1eb07f2dd600https://doi.org/10.1093/brain/awg077
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1A Worldwide Study of the Huntington's Disease Mutation: The Sensitivity and Specificity of Measuring CAG Repeats1994 · 604 citations
  2. 2Suicide risk in Huntington's disease.1993 · 138 citations
  3. 3Trinucleotide repeat length and progression of illness in Huntington's disease.1994 · 178 citations
  4. 4Homozygosity in Huntington’s disease1999 · 44 citations
  5. 5Molecular analysis of late onset Huntington's disease.1993 · 65 citations