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Mutation watch:PEX PLUS? Gene(s) for X-linked hypophosphatemia and deafness

dc.contributor.authorMeisler, Miriam H.en_US
dc.date.accessioned2006-09-08T20:00:58Z
dc.date.available2006-09-08T20:00:58Z
dc.date.issued1997-08en_US
dc.identifier.citationMeisler, Miriam; (1997). "Mutation watch:PEX PLUS? Gene(s) for X-linked hypophosphatemia and deafness." Mammalian Genome 8(8): 543-544. <http://hdl.handle.net/2027.42/42143>en_US
dc.identifier.issn0938-8990en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/42143
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=9250856&dopt=citationen_US
dc.format.extent28931 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.titleMutation watch:PEX PLUS? Gene(s) for X-linked hypophosphatemia and deafnessen_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, Ann Arbor, Michigan 48109-0618, USA, USen_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.identifier.pmid9250856en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/42143/1/335-8-8-543_8n8p543.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1007/s003359900499en_US
dc.identifier.sourceMammalian Genomeen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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