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Brief Correspondence

Yugoslav HD Phenocopies Analyzed on the Presence of Mutations in Prp, Ferritin, and Jp-3 Genes

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Pages 299-301 | Received 06 May 2004, Published online: 07 Jul 2009

References

  • Curtis A. R. J., Fey C., Morris C. M., et al. Mutation in the gene encoding ferritin light polypeptide causes dominant adult-onset basal ganglia disease. Nat Genet 2001; 1–5
  • Holmes S. E., O'Hearn E., Rosenblatt A., et al. A repeat expansion in the gene encoding junctophilin-3 is associated with Huntington disease. Nat Genet 2001; 29: 377–378, [CROSSREF]
  • Huntington's Disease Collaborative Research Group. A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes. Cell 1993; 72: 971–983, [CROSSREF]
  • Moore R. C., Xiang F., Monaghan J., et al. Huntington disease phenocopy is a familial prion disease. American Journal of Human Genetics 2001; 69: 1385–1388, [CROSSREF]

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