Skip to main content
NCBI home page
American Journal of Human Genetics logoLink to American Journal of Human Genetics
letter
. 1995 Aug;57(2):508–511.

Normal CAG repeat variation at the DRPLA locus in world populations.

R Deka, T Miki, S J Yin, S T McGarvey, M D Shriver, C H Bunker, S Raskin, J Hundrieser, R E Ferrell, R Chakraborty
PMCID: PMC1801546  PMID: 7668279

Full text

PDF
508

Selected References

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

  1. Aoki M., Abe K., Kameya T., Watanabe M., Itoyama Y. Maternal anticipation of DRPLA. Hum Mol Genet. 1994 Jul;3(7):1197–1198. doi: 10.1093/hmg/3.7.1197. [DOI] [PubMed] [Google Scholar]
  2. Burke J. R., Ikeuchi T., Koide R., Tsuji S., Yamada M., Pericak-Vance M. A., Vance J. M. Dentatorubral-pallidoluysian atrophy and Haw River syndrome. Lancet. 1994 Dec 17;344(8938):1711–1712. doi: 10.1016/s0140-6736(94)90497-9. [DOI] [PubMed] [Google Scholar]
  3. Burke J. R., Wingfield M. S., Lewis K. E., Roses A. D., Lee J. E., Hulette C., Pericak-Vance M. A., Vance J. M. The Haw River syndrome: dentatorubropallidoluysian atrophy (DRPLA) in an African-American family. Nat Genet. 1994 Aug;7(4):521–524. doi: 10.1038/ng0894-521. [DOI] [PubMed] [Google Scholar]
  4. Goldberg Y. P., Kremer B., Andrew S. E., Theilmann J., Graham R. K., Squitieri F., Telenius H., Adam S., Sajoo A., Starr E. Molecular analysis of new mutations for Huntington's disease: intermediate alleles and sex of origin effects. Nat Genet. 1993 Oct;5(2):174–179. doi: 10.1038/ng1093-174. [DOI] [PubMed] [Google Scholar]
  5. Goldman A., Ramsay M., Jenkins T. Absence of myotonic dystrophy in southern African Negroids is associated with a significantly lower number of CTG trinucleotide repeats. J Med Genet. 1994 Jan;31(1):37–40. doi: 10.1136/jmg.31.1.37. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Hirayama K., Takayanagi T., Nakamura R., Yanagisawa N., Hattori T., Kita K., Yanagimoto S., Fujita M., Nagaoka M., Satomura Y. Spinocerebellar degenerations in Japan: a nationwide epidemiological and clinical study. Acta Neurol Scand Suppl. 1994;153:1–22. doi: 10.1111/j.1600-0404.1994.tb05401.x. [DOI] [PubMed] [Google Scholar]
  7. Iizuka R., Hirayama K., Maehara K. A. Dentato-rubro-pallido-luysian atrophy: a clinico-pathological study. J Neurol Neurosurg Psychiatry. 1984 Dec;47(12):1288–1298. doi: 10.1136/jnnp.47.12.1288. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Imbert G., Kretz C., Johnson K., Mandel J. L. Origin of the expansion mutation in myotonic dystrophy. Nat Genet. 1993 May;4(1):72–76. doi: 10.1038/ng0593-72. [DOI] [PubMed] [Google Scholar]
  9. Koide R., Ikeuchi T., Onodera O., Tanaka H., Igarashi S., Endo K., Takahashi H., Kondo R., Ishikawa A., Hayashi T. Unstable expansion of CAG repeat in hereditary dentatorubral-pallidoluysian atrophy (DRPLA). Nat Genet. 1994 Jan;6(1):9–13. doi: 10.1038/ng0194-9. [DOI] [PubMed] [Google Scholar]
  10. 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]
  11. Myers R. H., MacDonald M. E., Koroshetz W. J., Duyao M. P., Ambrose C. M., Taylor S. A., Barnes G., Srinidhi J., Lin C. S., Whaley W. L. De novo expansion of a (CAG)n repeat in sporadic Huntington's disease. Nat Genet. 1993 Oct;5(2):168–173. doi: 10.1038/ng1093-168. [DOI] [PubMed] [Google Scholar]
  12. Nagafuchi S., Yanagisawa H., Sato K., Shirayama T., Ohsaki E., Bundo M., Takeda T., Tadokoro K., Kondo I., Murayama N. Dentatorubral and pallidoluysian atrophy expansion of an unstable CAG trinucleotide on chromosome 12p. Nat Genet. 1994 Jan;6(1):14–18. doi: 10.1038/ng0194-14. [DOI] [PubMed] [Google Scholar]
  13. Naito H., Oyanagi S. Familial myoclonus epilepsy and choreoathetosis: hereditary dentatorubral-pallidoluysian atrophy. Neurology. 1982 Aug;32(8):798–807. doi: 10.1212/wnl.32.8.798. [DOI] [PubMed] [Google Scholar]
  14. Neville C. E., Mahadevan M. S., Barceló J. M., Korneluk R. G. High resolution genetic analysis suggests one ancestral predisposing haplotype for the origin of the myotonic dystrophy mutation. Hum Mol Genet. 1994 Jan;3(1):45–51. doi: 10.1093/hmg/3.1.45. [DOI] [PubMed] [Google Scholar]
  15. SMITH J. K., GONDA V. E., MALAMUD N. Unusual form of cerebellar ataxia; combined dentato-rubral and pallido-Luysian degeneration. Neurology. 1958 Mar;8(3):205–209. doi: 10.1212/wnl.8.3.205. [DOI] [PubMed] [Google Scholar]
  16. Warner T. T., Williams L., Harding A. E. DRPLA in Europe. Nat Genet. 1994 Mar;6(3):225–225. doi: 10.1038/ng0394-225a. [DOI] [PubMed] [Google Scholar]

Articles from American Journal of Human Genetics are provided here courtesy of American Society of Human Genetics

RESOURCES