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Substitute consent to data sharing: a way forward for international dementia research?
A deluge of genetic and health-related data is being generated about patients with dementia. International sharing of these data accelerates dementia research. Seeking consent to data sharing is a challenge for dementia research where patients have lost or risk losing legal capacity. The laws of mos...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Oxford University Press
2017
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5570693/ https://www.ncbi.nlm.nih.gov/pubmed/28852560 http://dx.doi.org/10.1093/jlb/lsw063 |