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. 1995 Oct;57(4):972–975.

Localization of the candidate gene D-amino acid oxidase outside the refined I-cM region of spinocerebellar ataxia 2.

S Gispert, A Lunkes, N Santos, G Orozco, D Ha-Hao, T Ratzlaff, J Aguiar, I Torrens, L Heredero, A Brice, et al.
PMCID: PMC1801506  PMID: 7573064

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Selected References

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

  1. Auburger G., Diaz G. O., Capote R. F., Sanchez S. G., Perez M. P., del Cueto M. E., Meneses M. G., Farrall M., Williamson R., Chamberlain S. Autosomal dominant ataxia: genetic evidence for locus heterogeneity from a Cuban founder-effect population. Am J Hum Genet. 1990 Jun;46(6):1163–1177. [PMC free article] [PubMed] [Google Scholar]
  2. Belal S., Cancel G., Stevanin G., Hentati F., Khati C., Ben Hamida C., Auburger G., Agid Y., Ben Hamida M., Brice A. Clinical and genetic analysis of a Tunisian family with autosomal dominant cerebellar ataxia type 1 linked to the SCA2 locus. Neurology. 1994 Aug;44(8):1423–1426. doi: 10.1212/wnl.44.8.1423. [DOI] [PubMed] [Google Scholar]
  3. Fukui K., Miyake Y. Molecular cloning and chromosomal localization of a human gene encoding D-amino-acid oxidase. J Biol Chem. 1992 Sep 15;267(26):18631–18638. [PubMed] [Google Scholar]
  4. Gispert S., Twells R., Orozco G., Brice A., Weber J., Heredero L., Scheufler K., Riley B., Allotey R., Nothers C. Chromosomal assignment of the second locus for autosomal dominant cerebellar ataxia (SCA2) to chromosome 12q23-24.1. Nat Genet. 1993 Jul;4(3):295–299. doi: 10.1038/ng0793-295. [DOI] [PubMed] [Google Scholar]
  5. Gyapay G., Morissette J., Vignal A., Dib C., Fizames C., Millasseau P., Marc S., Bernardi G., Lathrop M., Weissenbach J. The 1993-94 Généthon human genetic linkage map. Nat Genet. 1994 Jun;7(2 Spec No):246–339. doi: 10.1038/ng0694supp-246. [DOI] [PubMed] [Google Scholar]
  6. Harding A. E. Classification of the hereditary ataxias and paraplegias. Lancet. 1983 May 21;1(8334):1151–1155. doi: 10.1016/s0140-6736(83)92879-9. [DOI] [PubMed] [Google Scholar]
  7. Hernández A., Magariño C., Gispert S., Santos N., Lunkes A., Orozco G., Heredero L., Beckmann J., Auburger G. Genetic mapping of the spinocerebellar ataxia 2 (SCA2) locus on chromosome 12q23-q24.1. Genomics. 1995 Jan 20;25(2):433–435. doi: 10.1016/0888-7543(95)80043-l. [DOI] [PubMed] [Google Scholar]
  8. Lopes-Cendes I., Andermann E., Rouleau G. A. Evidence for the existence of a fourth dominantly inherited spinocerebellar ataxia locus. Genomics. 1994 May 1;21(1):270–274. doi: 10.1006/geno.1994.1257. [DOI] [PubMed] [Google Scholar]
  9. Meldrum B., Garthwaite J. Excitatory amino acid neurotoxicity and neurodegenerative disease. Trends Pharmacol Sci. 1990 Sep;11(9):379–387. doi: 10.1016/0165-6147(90)90184-a. [DOI] [PubMed] [Google Scholar]
  10. Momoi K., Fukui K., Watanabe F., Miyake Y. Molecular cloning and sequence analysis of cDNA encoding human kidney D-amino acid oxidase. FEBS Lett. 1988 Sep 26;238(1):180–184. doi: 10.1016/0014-5793(88)80252-7. [DOI] [PubMed] [Google Scholar]
  11. Montgomery K. T., LeBlanc J. M., Tsai P., McNinch J. S., Ward D. C., de Jong P. J., Kucherlapati R., Krauter K. S. Characterization of two chromosome 12 cosmid libraries and development of STSs from cosmids mapped by FISH. Genomics. 1993 Sep;17(3):682–693. doi: 10.1006/geno.1993.1390. [DOI] [PubMed] [Google Scholar]
  12. Orozco Diaz G., Nodarse Fleites A., Cordovés Sagaz R., Auburger G. Autosomal dominant cerebellar ataxia: clinical analysis of 263 patients from a homogeneous population in Holguín, Cuba. Neurology. 1990 Sep;40(9):1369–1375. doi: 10.1212/wnl.40.9.1369. [DOI] [PubMed] [Google Scholar]
  13. Plaitakis A., Berl S., Yahr M. D. Abnormal glutamate metabolism in an adult-onset degenerative neurological disorder. Science. 1982 Apr 9;216(4542):193–196. doi: 10.1126/science.6121377. [DOI] [PubMed] [Google Scholar]
  14. Pulst S. M., Nechiporuk A., Starkman S. Anticipation in spinocerebellar ataxia type 2. Nat Genet. 1993 Sep;5(1):8–10. doi: 10.1038/ng0993-8c. [DOI] [PubMed] [Google Scholar]

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