Skip to content

ASF_Podcast_CoverArt-768x768

Resources

Understanding the UBE3A Gene

Resource Type:

Search ...

Home

Register your family

About
What is Angelman syndrome?

Symptoms

Causes

Diagnosis & Tests

Treatment & Care

Angelman Syndrome Foundation

Our History

Board of Directors

Committees & Groups

Play Video
Research
Angelman Syndrome Research

Types of Research

ASF Funded Research

Call For Proposals

Research Studies 101

Participate in a Study

Active Studies

For Industry

Published Articles

Clinical Trials 101

Treatments & Therapies

Phases & Therapeutic Pipeline

Find a Clinical Trial
Make an Impact
Ways to Donate

Donate Online

Join the ASF Cure Club

Text to Give

Send Sunshine

Start a Fundraiser

Programs & Events

Tips & Tools

Meet Fundraisers

Partner with us

Volunteer Opportunities

Join a Group or Committee

Shop & Support
ASF Clinics
Find an ASF Clinic

Europe

North America

South America

The Middle East

For Families

Clinic Patient Survey

FAQs

Provider Registry

For Clinicians

Jacob Pritzker Fellowship

Clinical Care Tool Kit

Published Articles

Join the Network
Find Resources
Resource Library

Newly Diagnosed

Adults

Family Support

Search by Sub-Topic

Advocacy

Financial Planning & Support

Individualized Education Plan (IEP)

ASF Podcast
Events
Events Calendar

Angelman Strong

Conferences & Symposia

Chicago Marathon

Tell Us About Your Event
News & Blog
Contact Us

Register Your Family

ASF_Podcast_CoverArt-768x768

Resources

Understanding the UBE3A Gene

Resource Type:

Search ...

About
Research
Make an Impact
ASF Clinics
Find Resources
Events
News & Blog
Contact Us

2026 Angelman Syndrome Foundation.
All rights reserved.
3015 E. New York Street, Suite A2 #285
Aurora, IL 60504
(800) 432-6435
info@angelman.org

Medical, Family Support

Understanding the UBE3A Gene

Two single mothers of children with Angelman syndrome discuss what help looks like for them.

episode on Youtube

episode on Youtube

ASF Podcast Options

Share

Facebook Instagram Linkedin Rss Youtube X-twitter

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.

About ASF
Board of Directors
Newly Diagnosed
Volunteer
Contact Us

Financial Transparency
Privacy

2026 Angelman Syndrome Foundation. All rights reserved.
3015 E. New York Street, Suite A2 #285, Aurora, IL 60504
(800) 432-6435
info@angelman.org

2026 Angelman Syndrome Foundation.
All rights reserved.
3015 E. New York Street, Suite A2 #285
Aurora, IL 60504
(800) 432-6435
info@angelman.org