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Q31069543-A41818E6-FD3D-4440-8CB0-4349566B068C
Q31069543-A41818E6-FD3D-4440-8CB0-4349566B068C
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http://www.wikidata.org/entity/statement/Q31069543-A41818E6-FD3D-4440-8CB0-4349566B068C
'You should at least ask'. The expectations, hopes and fears of rare disease patients on large-scale data and biomaterial sharing for genomics research
P2860
Q31069543-A41818E6-FD3D-4440-8CB0-4349566B068C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q31069543-A41818E6-FD3D-4440-8CB0-4349566B068C
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1c9b5f980a129937c3e92bbd1b4c327686de3e1b
P2860
Guidance in social and ethical issues related to clinical, diagnostic care and novel therapies for hereditary neuromuscular rare diseases: "translating" the translational