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Over 1200 families are caring for a loved one with the rare disease ”SynGAP” resulting from a variant of the SYNGAP1 gene. This 10 minute weekly podcast is for them. A quick summary of the latest news in the space. The host is Mike Graglia, co-founder & managing director of the SynGAP Research Fund. SRF is a parent-led, all volunteer public charity in the US that strives to accelerate research into treatments for SYNGAP1 so that we can help our loved ones in a timeframe that matters. Learn more at https://www.syngapresearchfund.org/
Episodes
Friday Dec 10, 2021
Friday Dec 10, 2021
Episode 39 of #Syngap10 - December 10, 2021
- Isoform paper https://www.biorxiv.org/content/10.1101/2021.12.05.471306v1
- Treatment one year sooner https://www.syngapresearchfund.org/post/oneyearsooner
- Syngap merch https://www.syngapresearchfund.org/shop
- SRF’s Blog https://www.syngapresearchfund.org/blog
- Fundraise https://syngap.fund/give
- Sign up for #Ciitizen. https://Ciitizen.com/SYNGAP1
- What is SYNGAP1? https://www.syngapresearchfund.org/home/what-is-syngap1
- Sign up for this 10 minute #podcast #SYNGAP10 here https://syngap.fund/10
#TalentTuesday #volunteer #Syngap #epilepsy #autism #intellectualdisability #id #raredisease #epilepsyawareness #autismawareness #rarediseaseresearch #SynGAPResearchFund #CareAboutRare #PatientAdvocacy #GCchat #Neurology #Genetics
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