dc.contributor.author | Hansson, M. | |
dc.contributor.author | Lochmuller, H. | |
dc.contributor.author | Riess, O. | |
dc.contributor.author | Schaefer, F. | |
dc.contributor.author | Orth, M. | |
dc.contributor.author | Rubinstein, Y. | |
dc.contributor.author | Molster, C. | |
dc.contributor.author | Dawkins, Hugh | |
dc.contributor.author | Taruscio, D. | |
dc.contributor.author | Posada, M. | |
dc.contributor.author | Woods, S. | |
dc.date.accessioned | 2017-11-24T05:26:29Z | |
dc.date.available | 2017-11-24T05:26:29Z | |
dc.date.created | 2017-11-24T04:48:51Z | |
dc.date.issued | 2016 | |
dc.identifier.citation | Hansson, 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.uri | http://hdl.handle.net/20.500.11937/58552 | |
dc.identifier.doi | 10.1038/ejhg.2016.52 | |
dc.publisher | Nature Publishing Group | |
dc.title | The risk of re-identification versus the need to identify individuals in rare disease research. | |
dc.type | Journal Article | |
dcterms.source.volume | 24 | |
dcterms.source.number | 11 | |
dcterms.source.startPage | 1553 | |
dcterms.source.endPage | 1558 | |
dcterms.source.issn | 1476-5438 | |
dcterms.source.title | European Journal of Human Genetics | |
curtin.department | Centre for Population Health Research | |
curtin.accessStatus | Open access via publisher | |