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Holding personal information in a disease-specific register: the perspectives of people with multiple sclerosis and professionals on consent and access
- Dr W Baird, Section of Public Health, ScHARR, University of Sheffield, 219 Portobello, Sheffield S1 4DP, UK; w.o.baird{at}sheffield.ac.uk
Citation
Holding personal information in a disease-specific register: the perspectives of people with multiple sclerosis and professionals on consent and access
Publication history
- Received March 21, 2008
- Revised September 8, 2008
- Accepted October 6, 2008
- First published January 30, 2009.
Online issue publication
April 27, 2016
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Copyright information
2009 BMJ Publishing Group & Institute of Medical Ethics
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