Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/99477
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dc.contributor.authorMcintyre, C.en
dc.contributor.authorDerrick-Roberts, A.en
dc.contributor.authorByers, S.en
dc.contributor.authorAnson, D.en
dc.date.issued2014en
dc.identifier.citationJournal of Gene Medicine, 2014; 16(11-12):374-387en
dc.identifier.issn1099-498Xen
dc.identifier.issn1521-2254en
dc.identifier.urihttp://hdl.handle.net/2440/99477-
dc.description.abstractAbstract not availableen
dc.description.statementofresponsibilityChantelle McIntyre, Ainslie L. K. Derrick-Roberts, Sharon Byers, Donald S. Ansonen
dc.language.isoenen
dc.publisherWileyen
dc.rightsCopyright © 2014 John Wiley & Sons, Ltden
dc.subjectGene therapy; neurodegenerative disorder; viral vectoren
dc.titleCorrection of murine mucopolysaccharidosis type IIIA central nervous system pathology by intracerebroventricular lentiviral-mediated gene deliveryen
dc.typeJournal articleen
dc.identifier.rmid0030016566en
dc.identifier.doi10.1002/jgm.2816en
dc.identifier.pubid161138-
pubs.library.collectionMedicine publicationsen
pubs.library.teamDS05en
pubs.verification-statusVerifieden
pubs.publication-statusPublisheden
dc.identifier.orcidByers, S. [0000-0001-5576-3636]en
Appears in Collections:Medicine publications

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