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Editorial: Is heterozygosity for a Wilson's disease gene defect an important underlying cause of infantile and childhood copper toxicosis syndromes? Figure 1 reproduced with permission from Lippincott Williams and Wilkins. http://lww.com
dc.contributor.authorBrewer, George J.en_US
dc.date.accessioned2006-04-19T14:06:18Z
dc.date.available2006-04-19T14:06:18Z
dc.date.issued2000en_US
dc.identifier.citationBrewer, George J. (2000)."Editorial: Is heterozygosity for a Wilson's disease gene defect an important underlying cause of infantile and childhood copper toxicosis syndromes? Figure 1 reproduced with permission from Lippincott Williams and Wilkins. http://lww.com ." The Journal of Trace Elements in Experimental Medicine 13(3): 249-254. <http://hdl.handle.net/2027.42/35050>en_US
dc.identifier.issn0896-548Xen_US
dc.identifier.issn1520-670Xen_US
dc.identifier.urihttps://hdl.handle.net/2027.42/35050
dc.description.abstractNo abstract.en_US
dc.format.extent82552 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherJohn Wiley & Sons, Inc.en_US
dc.subject.otherLife and Medical Sciencesen_US
dc.subject.otherMiscellaneous Medicalen_US
dc.titleEditorial: Is heterozygosity for a Wilson's disease gene defect an important underlying cause of infantile and childhood copper toxicosis syndromes? Figure 1 reproduced with permission from Lippincott Williams and Wilkins. http://lww.comen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelBiological Chemistryen_US
dc.subject.hlbsecondlevelChemical Engineeringen_US
dc.subject.hlbsecondlevelChemistryen_US
dc.subject.hlbsecondlevelPublic Healthen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelEngineeringen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartments of Human Genetics and Internal Medicine, University of Michigan, Ann Arbor, Michigan ; The University of Michigan Medical School, Department of Human Genetics, 4708 Medical Science II, Ann Arbor, MI 48109-0618en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/35050/1/1_ftp.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1002/1520-670X(2000)13:3<249::AID-JTRA1>3.0.CO;2-Len_US
dc.identifier.sourceThe Journal of Trace Elements in Experimental Medicineen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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