Knowing the answer opens up the world! #GeneticTesting #SYNGAP1 #Undiagnosed

curesyngap1.org

#Overexpression of SYNGAP1 suppresses the proliferation of #rectal adenocarcinoma via Wnt/β-Catenin signaling pathway: interesting paper published in Discover #Oncology .

link.springer.com/article/10.100…

Haciendo difusión 🔊 de #CADASIL en la jornada organizada por Sant Pau - Campus Salut Barcelona, junto con Elena Muiño MD PhD, Epilepsia Transversal y otras asociaciones como la de #SYNGAP1 ⚡️

#JuntosPorUnaCura

#syngap1 , carrera solidaria

Tomorrow, I will abseil down Anfield stadium in Liverpool to raise money for Patrick Wild Centre for the study of SYNGAP1, a genetic disorder my granddaughter suffers from.

I spoke with Matt Chorley about why I am raising money.

Please donate what you can here gofundme.com/f/syngap1resea…

Thanks to all those who abseiled down Anfield today to raise funds for #syngap1 research, including our very own L Mizen pictured here!

This weekend, I’m abseiling off Anfield Stadium to raise money for Patrick Wild Centre, for the study of SYNGAP1, a genetic disorder that my granddaughter suffers from.

Please donate what you can here 👇🏻
gofundme.com/f/syngap1resea…

There’s still time to donate before I abseil off Anfield Stadium on Sunday to raise money for Patrick Wild Centre, for the study of SYNGAP1, a genetic disorder that my granddaughter suffers from.

Please donate what you can here 👇🏻
gofundme.com/f/syngap1resea…

Help Fund SYNGAP1 Syndrome Research gofund.me/49302d48

Majadahonda ha celebrado esta mañana la II Carrera Solidaria en favor de la enfermedad poco frecuente Syngap1.
Enhorabuena tanto a los organizadores como a los participantes por una jornada llena de buenos valores.

🌟 Exciting news! 🎉

I’m excited to kickoff of SYNGAP1 Awareness Month with a Martha Lewis and her daughter Annie Peck, the first child in Nova Scotia identified with SYNGAP1-related disorders sharing her story.

Join us at the Wagmatcook Cultural & Heritage Centre, hosted by…

'You don't have to apologize for your child ever ... you don't have to expect them to be anything but how amazing they are!'

Ep 28 of #SYNGAP1Stories ! Available at Syngap.Fund/Stories or wherever you listen to podcasts.

#Syngap1 #SYNGAP1Stories Hope

Drug Repurposing is coming for #SYNGAP1 ! In our very first Drug Repurpose update, we look at N-acetyl-L-leucine (NALL). Syngap.Fund/NALL24

Clement Chow

In case you missed the premiere, #ConnectionIsEverything is on #YouTube ! YouTube.com/cureSYNGAP1

Details - Syngap.Fund/Jaxon

#SYNGAP1

Good luck Lindsay and to everyone else doing the #syngap1 abseil tomorrow

#Sprint4SynGAP in Fairfield for #TeamKaia yesterday was awesome. Three dads and lots of SynGAP Research Fund (SRF) merch in this shot.

We have $10k let to hit our goal, you can still bring us closer to a cure for #SYNGAP1 , donate now!
givebutter.com/ALjJXJ

Less than a week to go before we #SprintForSyngap ! Create your team ... Donate ... Help us find a cure! #EveryDollarMatters #SYNGAP1 #SprintForOurKids #EveryStepCounts

Syngap.Fund/Sprint24

¡Nuevo episodio de podcast! Episodio 14 - Diana Ramirez y Su Hija Luhana Desde Perú

Syngap.Fund/Cafe

#SYNGAP1 #CafeSYNGAP1

Vicky Arteaga

Details of Syngap1 and DD’s charity abseil here: gofund.me/ab7b817e
David Davis

A huge thank you to all the #SYNGAP1 families for organising this, allowing me to join in and of course the amazing fundraising effort. It was lovely to spend time with you all! Sarah Schofield David Davis Patrick Wild Centre