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The role of molecular testing and enzyme analysis in the management of hypomorphic citrullinemia
dc.contributor.authorDimmock, David P.en_US
dc.contributor.authorTrapane, Pamelaen_US
dc.contributor.authorFeigenbaum, Annetteen_US
dc.contributor.authorKeegan, Catherine E.en_US
dc.contributor.authorCederbaum, Stephenen_US
dc.contributor.authorGibson, Jamesen_US
dc.contributor.authorGambello, Michael J.en_US
dc.contributor.authorVaux, Keithen_US
dc.contributor.authorWard, Patriciaen_US
dc.contributor.authorO'Brien, William E.en_US
dc.contributor.authorFang, Pingen_US
dc.date.accessioned2010-04-14T20:03:40Z
dc.date.available2011-03-01T16:26:45Zen_US
dc.date.issued2010-04en_US
dc.identifier.citationDimmock, David P.; Trapane, Pamela; Feigenbaum, Annette; Keegan, Catherine E.; Cederbaum, Stephen; Gibson, James; Gambello, Michael J.; Vaux, Keith; Ward, Patricia; O'Brien, William E.; Fang, Ping (2010). "The role of molecular testing and enzyme analysis in the management of hypomorphic citrullinemia How to cite this article: Dimmock DP, Trapane P, Feigenbaum A, Keegan CE, Cederbaum S, Gibson J, Gambello MJ, Vaux K, Ward P, O'Brien WE, Fang P. 2010. The role of molecular testing and enzyme analysis in the management of hypomorphic citrullinemia. Am J Med Genet Part A 152A:1061. ." American Journal of Medical Genetics Part A 152A(4): 1061-1061. <http://hdl.handle.net/2027.42/69185>en_US
dc.identifier.issn1552-4825en_US
dc.identifier.issn1552-4833en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/69185
dc.description.abstractNo Abstract.en_US
dc.format.extent41987 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.publisherWiley Subscription Services, Inc., A Wiley Companyen_US
dc.subject.otherLife and Medical Sciencesen_US
dc.subject.otherGeneticsen_US
dc.titleThe role of molecular testing and enzyme analysis in the management of hypomorphic citrullinemiaen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelGeneticsen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDivision of Genetics, Department of Pediatrics, University of Michigan, Ann Arbor, Michiganen_US
dc.contributor.affiliationotherMolecular and Human Genetics, Baylor College of Medicine, Houston, Texas ; Division of Genetics, Department of Pediatrics, Medical College of Wisconsin, HRC Rm H5865, 8701 Watertown Plank Rd, Milwaukee, WI 53226.en_US
dc.contributor.affiliationotherGenetics Center, Department of Pediatrics, Medical College of Wisconsin, Milwaukee, Wisconsinen_US
dc.contributor.affiliationotherDivision of Genetics, The Hospital for Sick Children, Toronto, Ontario, Canadaen_US
dc.contributor.affiliationotherDepartments of Psychiatry, Pediatrics and Human Genetics, UCLA, Los Angeles, Californiaen_US
dc.contributor.affiliationotherUniversity of Texas Health Science Center at San Antonio, San Antonio, Texasen_US
dc.contributor.affiliationotherThe University of Texas Medical School at Houston, Houston, Texasen_US
dc.contributor.affiliationotherDepartment of Pediatrics, University of California San Diego, San Diego, Californiaen_US
dc.contributor.affiliationotherMolecular and Human Genetics, Baylor College of Medicine, Houston, Texasen_US
dc.contributor.affiliationotherMolecular and Human Genetics, Baylor College of Medicine, Houston, Texasen_US
dc.contributor.affiliationotherMolecular and Human Genetics, Baylor College of Medicine, Houston, Texasen_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/69185/1/33256_ftp.pdf
dc.identifier.doi10.1002/ajmg.a.33256en_US
dc.identifier.sourceAmerican Journal of Medical Genetics Part Aen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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