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An African-American cystic fibrosis patient homozygous for a novel frameshift mutation associated with reduced CFTR mRNA levels
dc.contributor.authorSmit, Lisa S.en_US
dc.contributor.authorNasr, Samya Z.en_US
dc.contributor.authorIannuzzi, Michael C.en_US
dc.contributor.authorCollins, Francis S.en_US
dc.date.accessioned2006-04-28T17:05:26Z
dc.date.available2006-04-28T17:05:26Z
dc.date.issued1993en_US
dc.identifier.citationSmit, Lisa S.; Nasr, Samya Z.; Iannuzzi, Michael C.; Collins, Francis S. (1993)."An African-American cystic fibrosis patient homozygous for a novel frameshift mutation associated with reduced CFTR mRNA levels." Human Mutation 2(2): 148-151. <http://hdl.handle.net/2027.42/38581>en_US
dc.identifier.issn1059-7794en_US
dc.identifier.issn1098-1004en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/38581
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=7686423&dopt=citationen_US
dc.description.abstractNo Abstract.en_US
dc.format.extent335752 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.titleAn African-American cystic fibrosis patient homozygous for a novel frameshift mutation associated with reduced CFTR mRNA levelsen_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.affiliationumDepartment of Human Genetics, University of Michigan, Ann Arbor, Michigan 48109en_US
dc.contributor.affiliationumDepartment of Pediatrics, University of Michigan, Ann Arbor, Michigan 48109en_US
dc.contributor.affiliationumDepartment of Human Genetics, University of Michigan, Ann Arbor, Michigan 48109 ; Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan 48109 ; Howard Hughes Medical Institute, University of Michigan, Ann Arbor, Michigan 48109 ; Department of Human Genetics, University of Michigan, Ann Arbor, Michigan 48109en_US
dc.contributor.affiliationotherHenry Ford Hospital Detroit, Michigan 48202; Fax: 313-936-2888en_US
dc.identifier.pmid7686423en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/38581/1/1380020217_ftp.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1002/humu.1380020217en_US
dc.identifier.sourceHuman Mutationen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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