What is SYNGAP1?
The Hall Family SYNGAP1 Story
Family raising awareness to rare genetic disorder after daughter diagnosed
SYNGAP1 Parent/SRF Director Intro: Kali & LJ, October 2020
Our Son's Rare Genetic Disorder - Syngap1
Overcoming SYNGAP1: A Family's Journey of Hope & Resilience
What is SYNGAP1 | Rare Genetic Disorder | Special Needs Day in the Life | Diagnosis after 14 years
GERMAN - CELEBRATING CAREN - Eine seltene Krankheit - SYNGAP1 - Diagnose nach 64 Jahren.
Syngap1 Patient Voices: Beckett's Story
The Lipman Family Shares Kiera's SYNGAP1 Story at the 4th annual SRF Gala
What it’s like living with 1 working SYNGAP1 Gene!
Rare Disease Day 2022 - SYNGAP1
SynGAP Research Fund - Helen Bateup - Webinar on Syngap - #SYNGAP1 #SRFWebinar
SRF | SYNGAP1 Awareness Video From Naya's Family
SYNGAP1 Parent/SRF Director Intro: Suzanne & Brent, November 2022 - Jansen's Journey
Foundations Of Rare Syngap1
CURE SYNGAP1 Conference 2025: Science Day Session 3.5 | Disease models to advance SRD therapeutics
SynGAP1 Parents/SRF Development Director Introduction, May 2020
Leben mit Syngap (Deutsch, Lange Version)
CURE SYNGAP1 | Missense Webinar SMART Program
