Mapping, cloning and genetic characterization of the region containing the Wilson disease gene (Articolo in rivista)

Type
Label
  • Mapping, cloning and genetic characterization of the region containing the Wilson disease gene (Articolo in rivista) (literal)
Anno
  • 1993-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1038/ng1293-338 (literal)
Alternative label
  • Petrukhin K.; Fischer S.G.; Pirastu M.; Tanzi R.E.; Chernov I.; Devoto M.; Brzustowicz L.M.; Cayanis E.; Vitale E.; Russo J.J.; Matseoane D.; Boukhgalter B.; Wasco W.; Figus A.L.; Loudianos J.; Cao A.; Sternlieb I.; Evgrafov O.; Parano E. (1993)
    Mapping, cloning and genetic characterization of the region containing the Wilson disease gene
    in Nature genetics (Print)
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Petrukhin K.; Fischer S.G.; Pirastu M.; Tanzi R.E.; Chernov I.; Devoto M.; Brzustowicz L.M.; Cayanis E.; Vitale E.; Russo J.J.; Matseoane D.; Boukhgalter B.; Wasco W.; Figus A.L.; Loudianos J.; Cao A.; Sternlieb I.; Evgrafov O.; Parano E. (literal)
Pagina inizio
  • 338 (literal)
Pagina fine
  • 343 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#url
  • http://www.scopus.com/inward/record.url?eid=2-s2.0-0027427695&partnerID=q2rCbXpz (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 5 (literal)
Rivista
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroFascicolo
  • 4 (literal)
Note
  • Scopu (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • Department of Psychiatry, New York State Psychiatric Institute, Columbia University, 722 W 168th St., New York, NY 10032, United States (literal)
Titolo
  • Mapping, cloning and genetic characterization of the region containing the Wilson disease gene (literal)
Abstract
  • Wilson disease (WD) is an autosomal recessive disorder of copper transport which maps to chromosome 13q14.3. In pursuit of the WD gene, we developed yeast artificial chromosome and cosmid contigs, and microsatellite markers which span the WD gene region. Linkage disequilibrium and haplotype analysis of 115 WD families confined the disease locus to a single marker interval. A candidate cDNA clone was mapped to this interval which, as shown in the accompanying paper, is very likely the WD gene. Our haplotype and mutation analyses predict that approximately half of all WD mutations will be rare in the American and Russian populations. (literal)
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