Join the RDCRN Contact Registry - to be kept informed of new clinical trials in the Network
The Rare Disease Clinical Research Network is a consortium of doctors, nurses, research coordinators, and research labs throughout the U.S., working together to improve the lives of people with Angelman, Rett, and Prader-Willi Syndromes through research.Visit the website
http://rarediseasesnetwork.epi.usf.edu/arpwsc/
Join the RDCRN Contact Registry
https://rarediseasesnetwork.epi.usf.edu/rdnwebapp/registry/descriptionandpurpose.aspx?ownerid=12&diseasetype=10
