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

Bridge the Gap - SYNGAP: Patient Support

Rare Disease Report

SRF | Rare Disease Day 2023 Warriors

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Rare Disease Day 2021

SYNGAP1 Foundation

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

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

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

Rare Disease Report

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

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Rare Disease Day 2022 - SYNGAP1

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

SynGAP Research Fund - SRF - SYNGAP1 🧬 🧠

Overcoming challenges in research of pediatric rare neurological disorders

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

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

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Rare Disease Day 2023 was epic and you should have been there. Sprint and Webinar update. #S10e96

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Hattie Foster's SYNGAP1 Story, support the Syngap Research Fund

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SynGAP Research Fund - Dr Jimmy Holder - Deep phenotyping to human neurons - #SYNGAP1 #SRFWebinar

SynGAP Research Fund - SRF - SYNGAP1 🧬 🧠

SYNGAP1 Conference 2022 - Session 2(e1) S1 CLINICAL SPECTRUM FROM CIITIZEN DATABASE - Kim Wiltrout

SynGAP Research Fund - SRF - SYNGAP1 🧬 🧠