Improving the patient’s position in data collection

Ryan Fischer
Ryan Fischer
  • 2 hour duration

A series of presentation about data collection initiatives in the Duchenne and Becker muscular dystrophy community. The following panel discussion will be chaired by Ryan Fischer (Parent Project Muscular Dystrophy USA) and co-chaired by Elvina Sakellariou (Duchenne Data Foundation). Panelists include representatives from various neuromuscular communities.