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1987: Genetic Marker Identified

January 2, 1987

1987: Genetic Marker Identified Timelines: The History of Angelman Syndrome and the ASF

Neuren Releases Results from Phase 2 Clinical Trial of NNZ-2591
Ionis Releases Data from the Phase 1/2 Halos Clinical Trial
Ultragenyx Announces Successful End-of-Phase 2 Meeting with FDA
Researchers at UNC Chapel Hill Find New Potential Treatment for AS
Dubai Launches First Angelman Clinic in GCC
Ionis Announces Positive Results from Halos Phase 1/2a
Ultragenyx Announces Positive Interim Phase 1/2 Data from GTX-102
Family Advocates Urge Congress’ Support During Inaugural Angelman Syndrome (AS) Congressional Advocacy Day
Angelman Clinic opens at Cedars-Sinai Guerin Children’s
Angelman Clinic opens at Children’s Hospital of Philadelphia (CHOP)
ASF and .PROT partner to launch new Angelman Center for families in Poland
Roche Clinical Trial of Rugonersen in Angelman Syndrome
ASF Opens Application for its Inaugural Jacob Pritzker Fellowship
Canadian Angelman Syndrome Society is now ASF Canada
GFAS Ukraine and ASF partner to Launch Clinic in Ukraine
AngelmanUK and ASF partner to launch clinics in the UK
LADDER Database Receives Transformational Dataset from Ovid Therapeutics
ASF Partners with Families in UAE to Expand Clinical Network
ASF to Host Screening of Caregiver Documentary, Unseen
Angelman Syndrome Foundation and Dup15q Alliance partner to launch the LADDER Learning Network, showing continued dedication to research

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The Mission

The mission of the 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.

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