A report was authored by Rebecca D Burdine PhD and Erin Sheldon.
Reviewed for accuracy by Wen-Hann Tan, BMBS Children’s Hospital Boston, Boston MA
Also, see more about the Genetics of Angelman syndrome.
The mission of Angelman Syndrome Foundation is to advance the awareness and treatment of Angelman syndrome through education and information, research and support for individuals with Angelman syndrome, their families and other concerned parties. We exist to give all of them a reason to smile, with the ultimate goal of finding a cure.