#gnao1 #gnao1warrior #stichtinggnao1

Hoy 1 de octubre, es el Día Internacional del #Gnao1 #GNAO1awareness #diamundialdelgnao1 #yotambiennavegocongnao1espana Puedes ver el vídeo de GNAO1 España para conocer más de esta patología #EnfermedadesRaras youtube.com/watch?v=nLW16y…

Op naar meer bekendheid, meer onderzoek en daarmee een betere toekomst voor kinderen met GNAO1! #gnao1 #stichtinggnao1 #gnao1awareness

Leestip! Een mooi interview met de oprichter van #stichtinggnao1 en mama van Max. #gnao1warrior #gnao1awareness #gnao1 linda.nl/nieuws/intervi…

Today, over 60 families in Western Ukraine affected by Epidermolysis Bullosa safely received supplies of vital medicines and desperately needed materials. We are incredibly grateful to everyone who has made this operation possible!

Thank you to ALL involved in ongoing research projects supporting GNAO1 research. Harald Mikkers, PhD, Simone Martinelli, PhD, Vladimir Katanaev, PhD, Jana Valnohova, PhD, Inna Shomer, PhD, Xin Chen, PhD, Miguel Sena Esteves, PhD, Richard Neubig, MD, PhD, Kirill Martemyanov, PhD.

Thank you to the Bow Foundation for organising today’s GNAO1 International Virtual Conference. Keep a close eye on their website and YouTube channel for the recordings of the presentations.

Behandeling patient Crispr-cas op de radio uitgezonden. #crisprcas Amsterdam UMC nporadio1.nl/fragmenten/nie…

Er is weer een nieuwe nieuwsbrief vol GNAO1 nieuws! Lees ‘m hier 👉 mailchi.mp/eac9eb3fa328/n… #gnao1 #stichtinggnao1nl #gnao1awareness

Vandaag is het GNAO1 Awarenessday! De dag om meer bekendheid te vragen voor deze zeldzame mutatie die kan leiden tot ernstige epilepsie en/of bewegingsstoornissen. Please share & like 💜💙 #StichtingGNAO1NL, #GNAO1Warrior, #GNAO1Awareness, #HopeAlways, #StrongerTogether

Mutations in the #GNAO1 gene cause a syndrome charaterised by intellectual #disability, hypotonia and irregular muscle contractions, among other symptoms. We are looking for people affected by this mutations to connect them in #Share4Rare 👥 Contact us! bit.ly/S4R-Registrati…

🚨🚨🚨Funding Opportunity! The Bow Foundation & The Orphan Disease Center @ UPenn are seeking #grant applications to support research related to #GNAO1 Neurodevelopmental Disorder. LOIs are due March 3, 2023; APPLY TODAY!! Follow the link to learn more: ow.ly/zLRs50MMxu2 #RareDisease #rare

Check out the new research update on our website > gnao1.nl/1268-2/

Fantastische Koningsdagactie voor GNAO1 in Diemen! Kom ook in actie vandaag. De speciale flyer is te downloaden op onze site (gnao1.nl) bij de nieuwsberichten. #gnao1 #supportresearch

Finished 2 stimulating days of updates from researchers and clinicians (Day 1) and exchanges with families, therapists, the rehabilitation community and accessible game builders (Day 2) #GNAO1 European Conference 2023 Famiglie GNAO1 Stichting GNAO1 NL GNAO1 España GNAO1 Action Mondo GNAO1 UK

We feel inspired & empowered by the #GNAO1EU23 conference in Rome. We thank Famiglie GNAO1 for organizing this amazing event and we thank all clinicians, researchers, patientorganizations- & families that attended! #StrongerTogether #gnao1 #curegnao1 GNAO1 España

📢 Maria Sáez González, Kes Kloosterhuis, Laura van de Pol, Frank Baas, Harald Mikkers, "Phenotypic Diversity in GNAO1 Patients: A Comprehensive Overview of Variants and Phenotypes", Human Mutation, vol. 2023, Article ID 6628283, 16 pages, 2023. doi.org/10.1155/2023/6…