World's Largest Newborn Screening Study for Four Rare Disorders Launches
The Angelman Syndrome Foundation and the Foundation for Prader-Willi Research announce funding to support the world’s largest newborn screening study for four rare genetic disorders: Angelman, Prader-Willi, Fragile X and Dup15q syndromes. The Victorian Medical Research Acceleration Fund this year…
FPWR Researchers Publish Latest Results
The Foundation for Prader-Willi Research (FPWR) is pleased to share remarkable progress that has been made towards its mission of eliminating the challenges of Prader-Willi syndrome (PWS) and advancing therapeutic development. Two notable discoveries supported by FPWR have recently been…