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Q28485060-33CE81BA-8E42-4A93-92A2-2D51E1DB38EC
Q28485060-33CE81BA-8E42-4A93-92A2-2D51E1DB38EC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28485060-33CE81BA-8E42-4A93-92A2-2D51E1DB38EC
Guidance in social and ethical issues related to clinical, diagnostic care and novel therapies for hereditary neuromuscular rare diseases: "translating" the translational
P2860
Q28485060-33CE81BA-8E42-4A93-92A2-2D51E1DB38EC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28485060-33CE81BA-8E42-4A93-92A2-2D51E1DB38EC
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
ee5ece1c2d5027629d1de67afd340a3ad15cf684
P2860
Informed consent process for patient participation in rare disease registries linked to biorepositories