The risk of re-identification versus the need to identify individuals in rare disease research.

Hansson, M.; Lochmuller, H.; Riess, O.; Schaefer, F.; Orth, M.; Rubinstein, Y.; Molster, C.; Dawkins, Hugh; Taruscio, D.; Posada, M.; Woods, S.

doi:10.1038/ejhg.2016.52

Access Status

Open access via publisher

Authors

Hansson, M.

Lochmuller, H.

Riess, O.

Schaefer, F.

Orth, M.

Rubinstein, Y.

Molster, C.

Dawkins, Hugh

Taruscio, D.

Posada, M.

Woods, S.

Date

2016

Collection

Curtin Research Publications

Type

Journal Article

Metadata

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Abstract

No Abstract Available

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.

Source Title

European Journal of Human Genetics

URI

http://hdl.handle.net/20.500.11937/58552

DOI

10.1038/ejhg.2016.52

Department

Centre for Population Health Research