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Novel missense mutation (G314R) in a cystic fibrosis patient with hepatic failure
dc.contributor.authorNasr, Samya Z.en_US
dc.contributor.authorStrong, Theresa V.en_US
dc.contributor.authorMansoura, Monique K.en_US
dc.contributor.authorDawson, David C.en_US
dc.contributor.authorCollins, Francis S.en_US
dc.date.accessioned2006-04-28T17:05:32Z
dc.date.available2006-04-28T17:05:32Z
dc.date.issued1996en_US
dc.identifier.citationNasr, Samya Z.; Strong, Theresa V.; Mansoura, Monique K.; Dawson, David C.; Collins, Francis S. (1996)."Novel missense mutation (G314R) in a cystic fibrosis patient with hepatic failure." Human Mutation 7(2): 151-154. <http://hdl.handle.net/2027.42/38583>en_US
dc.identifier.issn1059-7794en_US
dc.identifier.issn1098-1004en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/38583
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=8829633&dopt=citationen_US
dc.description.abstractNo abstract.en_US
dc.format.extent367634 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherWiley Subscription Services, Inc., A Wiley Companyen_US
dc.subject.otherLife and Medical Sciencesen_US
dc.subject.otherGeneticsen_US
dc.titleNovel missense mutation (G314R) in a cystic fibrosis patient with hepatic failureen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelGeneticsen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.subject.hlbtoplevelScienceen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartments of Pediatrics, Human Genetics, Bioengineering, Physiology, and Internal Medicine, University of Michigan, Ann Arbor, Michigan 48109 ; Departments of Pediatrics, Human Genetics, Bioengineering, Physiology, and Internal Medicine, University of Michigan, Ann Arbor, Michigan 48109; Fax: 313-763-4208en_US
dc.contributor.affiliationumDepartments of Pediatrics, Human Genetics, Bioengineering, Physiology, and Internal Medicine, University of Michigan, Ann Arbor, Michigan 48109en_US
dc.contributor.affiliationumDepartments of Pediatrics, Human Genetics, Bioengineering, Physiology, and Internal Medicine, University of Michigan, Ann Arbor, Michigan 48109en_US
dc.contributor.affiliationumDepartments of Pediatrics, Human Genetics, Bioengineering, Physiology, and Internal Medicine, University of Michigan, Ann Arbor, Michigan 48109en_US
dc.contributor.affiliationumDepartments of Pediatrics, Human Genetics, Bioengineering, Physiology, and Internal Medicine, University of Michigan, Ann Arbor, Michigan 48109 ; National Center for Human Genome Research, Bethesda, Maryland 20892en_US
dc.identifier.pmid8829633en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/38583/1/10_ftp.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1002/(SICI)1098-1004(1996)7:2<151::AID-HUMU10>3.0.CO;2-1en_US
dc.identifier.sourceHuman Mutationen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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