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Location of the 9257 and ataxia mutations on mouse Chromosome 18
dc.contributor.authorHansen, G. M.en_US
dc.contributor.authorRadice, G. L.en_US
dc.contributor.authorGriffith, A. J.en_US
dc.contributor.authorMeisler, Miriam H.en_US
dc.contributor.authorJohnson, K. R.en_US
dc.contributor.authorDavisson, M. T.en_US
dc.contributor.authorBurgess, D. L.en_US
dc.contributor.authorJustice, M. J.en_US
dc.contributor.authorKohrman, David C.en_US
dc.date.accessioned2006-09-08T20:00:20Z
dc.date.available2006-09-08T20:00:20Z
dc.date.issued1996-06en_US
dc.identifier.citationGriffith, A.J.; Radice, G.L.; Burgess, D.L.; Kohrman, D.C.; Hansen, G.M.; Justice, M.J.; Johnson, K.R.; Davisson, M.T.; Meisler, M.H.; (1996). "Location of the 9257 and ataxia mutations on mouse Chromosome 18." Mammalian Genome 7(6): 417-419. <http://hdl.handle.net/2027.42/42133>en_US
dc.identifier.issn0938-8990en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/42133
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=8662222&dopt=citationen_US
dc.description.abstractThe location of three mutations on proximal Chromosome (Chr) 18 was determined by analysis of the offspring of several backcrosses. The results demonstrate that ataxia and the insertional mutation TgN9257Mm are separated by less than 1 cM and are located approximately 3 cM from the centromere, while the balding locus is 7 cM more distal. Previous data demonstrated that the twirler locus also maps within 1 cM of ataxia. The corrected locations will contribute to identification of appropriate candidate genes for these mutations. Two polymorphic microsatellite markers for proximal Chr 18 are described, D18Umi1 and D18Umi2. The Lama3 locus encoding the α3 subunit of nicein was mapped distal to ataxia and did not recombine with Tg9257.en_US
dc.format.extent79618 bytes
dc.format.extent3115 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherSpringer-Verlag; Springer-Verlag New York Inc.en_US
dc.subject.otherLegacyen_US
dc.titleLocation of the 9257 and ataxia mutations on mouse Chromosome 18en_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelNatural Resources and Environmenten_US
dc.subject.hlbsecondlevelMolecular, Cellular and Developmental Biologyen_US
dc.subject.hlbsecondlevelEcology and Evolutionary Biologyen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.subject.hlbtoplevelScienceen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Human Genetics, 4708 Medical Science II, University of Michigan School of Medicine, Ann Arbor, Michigan 48109-0618, USA, USen_US
dc.contributor.affiliationumDepartment of Human Genetics, 4708 Medical Science II, University of Michigan School of Medicine, Ann Arbor, Michigan 48109-0618, USA, USen_US
dc.contributor.affiliationumDepartment of Human Genetics, 4708 Medical Science II, University of Michigan School of Medicine, Ann Arbor, Michigan 48109-0618, USA, USen_US
dc.contributor.affiliationumDepartment of Human Genetics, 4708 Medical Science II, University of Michigan School of Medicine, Ann Arbor, Michigan 48109-0618, USA, USen_US
dc.contributor.affiliationotherDepartment of Obstetrics & Gynecology, University of Pennsylvania, Philadelphia, Pennsylvania 19104, USA, USen_US
dc.contributor.affiliationotherThe Jackson Laboratory, Bar Harbor, Maine 04609, USA, USen_US
dc.contributor.affiliationotherDivision of Biology, Kansas State University, Manhattan, Kansas, USA, USen_US
dc.contributor.affiliationotherThe Jackson Laboratory, Bar Harbor, Maine 04609, USA, USen_US
dc.contributor.affiliationotherDivision of Biology, Kansas State University, Manhattan, Kansas, USA, USen_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.identifier.pmid8662222en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/42133/1/335-7-6-417_7n6p417.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1007/s003359900124en_US
dc.identifier.sourceMammalian Genomeen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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