New reading for the #syngap community! Hematopoietic stem cell gene therapy for the treatment of SYNGAP1‐related non‐specific intellectual disability - Anderson - 2024 - The Journal of Gene Medicine - Wiley Online Library ⁦CURE SYNGAP1 aka SynGAP Research Fund 501(C)(3)⁩ onlinelibrary.wiley.com/doi/full/10.10…

Long day but before it ends I have to thank CBER U.S. FDA for discussing Syngap1 with my co-sponsor Joe Anderson and me. Lots to unpack and share with the S1 community ASAP SYNGAP1 Global Network (SGN) Syngap Research Fund Australia CURE SYNGAP1 aka SynGAP Research Fund 501(C)(3) #syngap

In Australia? Support syngap research by buying a raffle ticket and be in with a chance to win a car. facebook.com/share/p/17QK8i…

Last chance to simultaneously help fund syngap reserach and buy a ticket to win a car! facebook.com/share/p/ex8EhE…

So what are the take-homes? Syngapians are SICK and the FDA sees that. Drug developers can pull this SDLT lever and justifiably streamline their work and urgently bring treatments to our loved ones with Syngap1 Syndrome. 10/x

Big news for those working on treatments for Syngap and for our community- clinical trials may not be as onerous as expected.

Amazing day one of the CURE SYNGAP1 aka SynGAP Research Fund 501(C)(3) scientific conference hanging out with families and researchers!

#SYNGAP1 @ AES 2024 CURE SYNGAP1 aka SynGAP Research Fund 501(C)(3) Virginie McNamar SYNGAP1 Global Network (SGN) Syngap Research Fund Australia #SYNGAPConf

The 7th Syngap conference preceded AES this year, here are our takeaways, m.facebook.com/story.php?stor…

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How many people have SYNGAP1? 4Q24 #SYNGAPcensus = 🌏1,530 Details: cureSYNGAP1.org/Census 🇺🇸432 🇬🇧128 🇩🇪126 🇨🇳113 🇫🇷99 🇳🇱55 🇪🇸53 🇮🇹52 🇦🇺45 🇵🇱44 🇨🇦41 🇷🇺33 🇧🇷32 🇰🇷22 🇦🇷16 🇨🇭15 🇳🇴🇸🇪🇨🇴13 🇩🇰🇧🇪12 🇮🇪11 🇮🇱10 🇵🇹🇯🇵🇨🇱9 🇹🇷8 🇸🇮7 🇫🇮🇮🇳6 🇷🇸🇲🇽5 🇪🇪🇧🇾🇦🇹🇪🇬🇺🇦🇨🇿🇬🇷🇷🇴4 🇩🇴🇭🇺🇦🇪3 🇭🇰🇸🇷🇲🇦🇲🇾🇧🇦🇸🇰🇸🇬🇭🇷2

SRF has published its first paper! We chronicle the last 5 years of advancements in specific treatments for SYNGAP1-related disorder and how #SynGAPResearchFund has helped accelerate the route to meaningful treatments for our loved ones living with #SYNGAP1.

Great day at the Port Fairy Marathon, raising awareness and funds for Syngap research. Plus a little help from Dan Tehan. facebook.com/share/p/19z6EG…

How many people have SYNGAP1? 1Q25 #SYNGAPcensus = 🌏1,581 Details: cureSYNGAP1.org/Census 🇺🇸 449 🇩🇪 129 🇬🇧 128 🇨🇳 114 🇫🇷 113 🇳🇱 55 🇪🇸 53 🇮🇹 52 🇦🇺 47 🇵🇱 45 🇨🇦 42 🇷🇺 34 🇧🇷 33 🇰🇷 22 🇦🇷 20 🇨🇭 15 🇳🇴🇸🇪🇨🇴 13 🇩🇰🇧🇪 12 🇮🇪 11 🇨🇱🇮🇱 10 🇵🇹🇯🇵 9 🇹🇷 8 🇸🇮 7 🇫🇮🇮🇳🇦🇹 6 🇷🇸🇲🇽 5 🇪🇪🇧🇾🇪🇬🇺🇦🇨🇿🇬🇷🇷🇴 4

facebook.com/share/p/18fr1v… Syngap session to educate, inspire and mobilise the Australian Syngap community

Today at #ASGCT2025, we shared new data showcasing increased #SYNGAP1 protein levels in non-human primates from our program aimed at addressing the unmet need in SYNGAP1-related disorders & more progress from our RAP Platform™. Catch up on our data: bit.ly/3GZa5vg $CAMP

Proud to be co-founders and part of Syngap Global Network, a collaboration of 18 syngap foundations across the globe! 💜💙💚 #splash4syngap #SGN #SYNGAP1 facebook.com/share/v/192XU6…

June 21 - International #SYNGAP1 Awareness day - #SPLASH4SYNGAP! 48 Australians are now diagnosed with #SYNGAP1 and growing! Find out more about #SYNGAP1 and #splash4syngap. #SGN facebook.com/share/r/16YVb1…

How many people have 𝘚𝘠𝘕𝘎𝘈𝘗𝟣? 2Q25 #SYNGAP1Census = 1,636 including first patients in Bulgaria, Pakistan, Paraguay, and Uruguay! Details👉 cureSYNGAP1.org/Census 🇺🇸 462 🇩🇪 133 🇬🇧 128 🇫🇷 123 🇨🇳 115 🇪🇸 59 🇳🇱🇮🇹 55 🇦🇺 47 🇵🇱 46 🇨🇦 42 🇷🇺 35 🇧🇷 34 🇰🇷 23 🇦🇷 21 🇨🇭 15 🇨🇴 14 🇳🇴🇸🇪

facebook.com/share/p/1G4YVC…