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dc.contributor.authorHansson, M.
dc.contributor.authorLochmuller, H.
dc.contributor.authorRiess, O.
dc.contributor.authorSchaefer, F.
dc.contributor.authorOrth, M.
dc.contributor.authorRubinstein, Y.
dc.contributor.authorMolster, C.
dc.contributor.authorDawkins, Hugh
dc.contributor.authorTaruscio, D.
dc.contributor.authorPosada, M.
dc.contributor.authorWoods, S.
dc.date.accessioned2017-11-24T05:26:29Z
dc.date.available2017-11-24T05:26:29Z
dc.date.created2017-11-24T04:48:51Z
dc.date.issued2016
dc.identifier.citationHansson, M. and Lochmuller, H. and Riess, O. and Schaefer, F. and Orth, M. and Rubinstein, Y. and Molster, C. et al. 2016. The risk of re-identification versus the need to identify individuals in rare disease research.. European Journal of Human Genetics. 24 (11): pp. 1553-1558.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/58552
dc.identifier.doi10.1038/ejhg.2016.52
dc.publisherNature Publishing Group
dc.titleThe risk of re-identification versus the need to identify individuals in rare disease research.
dc.typeJournal Article
dcterms.source.volume24
dcterms.source.number11
dcterms.source.startPage1553
dcterms.source.endPage1558
dcterms.source.issn1476-5438
dcterms.source.titleEuropean Journal of Human Genetics
curtin.departmentCentre for Population Health Research
curtin.accessStatusOpen access via publisher


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