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dc.contributor.authorNewman, Jeremy RB
dc.contributor.authorLehn, Alexander C
dc.contributor.authorBoyle, Richard S
dc.contributor.authorSilburn, Peter A
dc.contributor.authorMellick, George D
dc.date.accessioned2017-05-03T14:10:45Z
dc.date.available2017-05-03T14:10:45Z
dc.date.issued2013
dc.date.modified2014-04-15T22:58:02Z
dc.identifier.issn0885-3185
dc.identifier.doi10.1002/mds.25479
dc.identifier.urihttp://hdl.handle.net/10072/58534
dc.description.peerreviewedYes
dc.description.publicationstatusYes
dc.languageEnglish
dc.language.isoeng
dc.publisherJohn Wiley & Sons
dc.publisher.placeUnited States
dc.relation.ispartofstudentpublicationY
dc.relation.ispartofpagefrom1752
dc.relation.ispartofpageto1753
dc.relation.ispartofissue12
dc.relation.ispartofjournalMovement Disorders
dc.relation.ispartofvolume28
dc.rights.retentionY
dc.subject.fieldofresearchNeurology and Neuromuscular Diseases
dc.subject.fieldofresearchClinical Sciences
dc.subject.fieldofresearchHuman Movement and Sports Sciences
dc.subject.fieldofresearchNeurosciences
dc.subject.fieldofresearchcode110904
dc.subject.fieldofresearchcode1103
dc.subject.fieldofresearchcode1106
dc.subject.fieldofresearchcode1109
dc.titleScreening for rare sequence variants in the THAP1 gene in a primary dystonia cohort
dc.typeJournal article
dc.type.descriptionC1 - Articles
dc.type.codeC - Journal Articles
gro.rights.copyrightSelf-archiving of the author-manuscript version is not yet supported by this journal. Please refer to the journal link for access to the definitive, published version or contact the authors for more information.
gro.date.issued2013
gro.hasfulltextNo Full Text
gro.griffith.authorNewman, Jeremy R.
gro.griffith.authorMellick, George


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