Syngap Rare Neurological Condi

What Are SYNGAP Mutations?

Rare Disease Report

What are SYNGAP Mutations?

Rare Disease Report

Monica Weldon Discusses SYNGAP and the Role of Advocacy

Family raising awareness to rare genetic disorder after daughter diagnosed

SynGAP Research Fund - SRF - SYNGAP1 🧬 🧠

Bridge the Gap - SYNGAP: Patient Support

Rare Disease Report

SRF | Rare Disease Day 2023 Warriors

SynGAP Research Fund - SRF - SYNGAP1 🧬 🧠

Rare Disease Day 2021

SYNGAP1 Foundation

Rare Disease Day is Monday! And here at SRF we can feel it all happening… 🦓

SynGAP Research Fund - SRF - SYNGAP1 🧬 🧠

Rare Diseases and Getting Coverage for Medical and Behavioral Therapies - Its Complicated

Rare Disease Report

Rare Disease Day 2022 - SYNGAP1

SynGAP Research Fund - SRF - SYNGAP1 🧬 🧠

Celebrating Caren Trailer - A #RareDisease (#SYNGAP1) Diagnosis 64 Years in the Making

SynGAP Research Fund - SRF - SYNGAP1 🧬 🧠

Special Double Episode: Understanding your particular variant and what to do about it (Hint: #iPSC)🧫

SynGAP Research Fund - SRF - SYNGAP1 🧬 🧠

JR's book, ORCA & RareX, Data, Update Ciitizen, Syndrome Mgmt, ASOs for Brain, Libby&Espy #S10e89

SynGAP Research Fund - SRF - SYNGAP1 🧬 🧠

Our Son's Rare Genetic Disorder - Syngap1

F78.A1 is the ICD-10 code for 883 SynGAPians today! #UFDcure Cannonball in 5 days! - Episode 29 of #

SynGAP Research Fund - SRF - SYNGAP1 🧬 🧠

Breaking Down Barriers in Rare Disease Research: Advantages and Obstacles in Data Sharing

SynGAP Research Fund - SRF - SYNGAP1 🧬 🧠

New Grant, Rare Affair, SYNGAP1 research and events #S10e88

SynGAP Research Fund - SRF - SYNGAP1 🧬 🧠

International Syngap1 Conference 2020 AMENA SMITH FINE, MD PhD

SYNGAP1 Foundation

Why we need to keep talking about SYNGAP1 #S10e91

SynGAP Research Fund - SRF - SYNGAP1 🧬 🧠

Overcoming challenges in research of pediatric rare neurological disorders