Interview avec Ms Olivia NICLAS de l'Association Francais d'Ectodermal Dysplasia

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Uploaded by on Sep 29, 2009

Ms Olivia NICLAS from the French Association for Ectodermal Dysplasia took part in the Eurordis Summer School Training of Rare Disease Patient Advocates in Clinical Trials and Drug Development which took place in Barcelona at the Fundacio Dr. Robert in June 2009 with the support of the DIA, the European Commission and the AFM

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Nonprofits & Activism

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