Why we need to keep talking about SYNGAP1 #S10e91

Why we need to keep talking about SYNGAP1 #S10e91

Press is good! 
– Short link: https://syngap.fund/nw

– Long link: https://www.newsweek.com/my-son-syngap1-rare-genetic-condition-1776362

Jo Ashline in Invitae:
https://blog.invitae.com/finding-andrews-truth-a-family-s-unexpected-rare-disease-diagnosis-e21e97da6baf

Episode 90 was good, remember to listen, #S10e90 https://www.youtube.com/watch?v=Mp4jHg-GXjE

Ciitizen is over 200! Update your Ciitizen Records
– Sign-IN https://app.ciitizen.com/ 

– Sign-UP https://ciitizen.com/syngap1 

Conference Videos are up from Science Day!

https://www.syngapresearchfund.org/post/2022-syngap1-conference-roundtable

Grant applications due March 1, 2023

https://www.syngapresearchfund.org/professionals/grants/how-to-apply

Priority Areas:
– Biomarkers & Endpoints

 – VUS Resolution
– Characterizing SYNGAP1 patients in the literature

 – SYNGAP1 Translational Science

Help Research with this brief survey.  Tell a friend and share these links – 200 & counting, $50 each. 

– Short link: https://syngap.fund/UCSF_survey

– Long link: fd91u8h6784.typeform.com/to/cvMzzG9z?utm_source=advocacy_org&utm_medium=email&utm_campaign=predictive_tool_survey&utm_term=syngap_research_fund

This is a podcast: subscribe to and rate this 10 minute #podcast #SYNGAP10 here 

– https://www.syngapresearchfund.org/syngap10-podcast

Apple podcasts: 

– https://podcasts.apple.com/us/podcast/syngap10-weekly-10-minute-updates-on-syngap1-video/id1560389818

Episode 91 of #Syngap10 – January 31,  2023 

#epilepsy #autism #intellectualdisability #id #anxiety #raredisease #epilepsyawareness #autismawareness #rarediseaseresearch #SynGAPResearchFund #CareAboutRare #PatientAdvocacy #GCchat #Neurology #GeneChat