Skip to main content
NCBI home page
The BMJ logoLink to The BMJ
editorial
. 1993 Aug 14;307(6901):396–397. doi: 10.1136/bmj.307.6901.396

The gene for Huntington's disease.

A E Harding
PMCID: PMC1678428  PMID: 8374447

Full text

PDF
396

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Goldberg Y. P., Andrew S. E., Clarke L. A., Hayden M. R. A PCR method for accurate assessment of trinucleotide repeat expansion in Huntington disease. Hum Mol Genet. 1993 Jun;2(6):635–636. doi: 10.1093/hmg/2.6.635. [DOI] [PubMed] [Google Scholar]
  2. Gusella J. F., Wexler N. S., Conneally P. M., Naylor S. L., Anderson M. A., Tanzi R. E., Watkins P. C., Ottina K., Wallace M. R., Sakaguchi A. Y. A polymorphic DNA marker genetically linked to Huntington's disease. Nature. 1983 Nov 17;306(5940):234–238. doi: 10.1038/306234a0. [DOI] [PubMed] [Google Scholar]
  3. Harley H. G., Rundle S. A., Reardon W., Myring J., Crow S., Brook J. D., Harper P. S., Shaw D. J. Unstable DNA sequence in myotonic dystrophy. Lancet. 1992 May 9;339(8802):1125–1128. doi: 10.1016/0140-6736(92)90729-m. [DOI] [PubMed] [Google Scholar]
  4. Li S. H., McInnis M. G., Margolis R. L., Antonarakis S. E., Ross C. A. Novel triplet repeat containing genes in human brain: cloning, expression, and length polymorphisms. Genomics. 1993 Jun;16(3):572–579. doi: 10.1006/geno.1993.1232. [DOI] [PubMed] [Google Scholar]
  5. MacDonald M. E., Haines J. L., Zimmer M., Cheng S. V., Youngman S., Whaley W. L., Wexler N., Bucan M., Allitto B. A., Smith B. Recombination events suggest potential sites for the Huntington's disease gene. Neuron. 1989 Aug;3(2):183–190. doi: 10.1016/0896-6273(89)90031-7. [DOI] [PubMed] [Google Scholar]
  6. Orr H. T., Chung M. Y., Banfi S., Kwiatkowski T. J., Jr, Servadio A., Beaudet A. L., McCall A. E., Duvick L. A., Ranum L. P., Zoghbi H. Y. Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1. Nat Genet. 1993 Jul;4(3):221–226. doi: 10.1038/ng0793-221. [DOI] [PubMed] [Google Scholar]
  7. Riess O., Noerremoelle A., Soerensen S. A., Epplen J. T. Improved PCR conditions for the stretch of (CAG)n repeats causing Huntington's disease. Hum Mol Genet. 1993 Jun;2(6):637–637. doi: 10.1093/hmg/2.6.637. [DOI] [PubMed] [Google Scholar]
  8. Riggins G. J., Lokey L. K., Chastain J. L., Leiner H. A., Sherman S. L., Wilkinson K. D., Warren S. T. Human genes containing polymorphic trinucleotide repeats. Nat Genet. 1992 Nov;2(3):186–191. doi: 10.1038/ng1192-186. [DOI] [PubMed] [Google Scholar]
  9. Suthers G. K., Huson S. M., Davies K. E. Instability versus predictability: the molecular diagnosis of myotonic dystrophy. J Med Genet. 1992 Nov;29(11):761–765. doi: 10.1136/jmg.29.11.761. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Valdes J. M., Tagle D. A., Elmer L. W., Collins F. S. A simple non-radioactive method for diagnosis of Huntington's disease. Hum Mol Genet. 1993 Jun;2(6):633–634. doi: 10.1093/hmg/2.6.633. [DOI] [PubMed] [Google Scholar]

Articles from BMJ : British Medical Journal are provided here courtesy of BMJ Publishing Group

RESOURCES