Researchers are inviting individuals with a #SCN1B genetic variant to take part in a short online survey to learn more about the experiences of people with SCN1B.

Want to help? Complete the 10‑minute survey: https://redcap.link/ftykr35s

#EpilepsyResearch #RareDisease #Genetics

We’re inviting individuals with a #SCN1B genetic variant to take part in an online survey led by the University of Bristol. Your input will help improve understanding and support for families affected by SCN1B.

Click here to take part: https://redcap.link/ftykr35s