Conecte-se e aprenda! As redes regionais e variantes são o seu lugar para suporte ao vivo e atualizações de pesquisa. As redes SCN8A, patrocinadas pela SCN8A Alliance, oferecem oportunidades trimestrais de contato com o Dr. Hammer, um pai SCN8A e o cientista genético responsável pela descoberta da associação do gene SCN8A com a epilepsia pediátrica. …
This variant meets the second Saturday of March, June, September, and December to discuss what’s new with SCN8A. Please join us to learn more and meet other families with your variant! Register here!
加入这个地区会议，讨论 SCN8A 的新功能。请加入我们以了解更多信息并结识您所在地区的其他家庭！ Join this region meeting to discuss what’s new with SCN8A. Please join us to learn more and meet other families in your region! 在这里注册 Register here!
This region meets the third Wednesday of March, June, September, and December to discuss what's new with SCN8A. Please join us to learn more and meet other families in your region! Register here!
Join us to hear from SCN8A parents and researchers, Madeleine Oudin and Chris Burge, to learn about different kinds of emerging genetic therapies, what is in the pipeline for SCN8A and hear about their journey to find an ASO treatment for their daughter, Margot, with a new company called nLorem. You can register in advance …
Emerging Genetic Treatments for SCN8A and a look at n-of-1/nLorem Read More »
This group meets on the fourth Saturday of March, June, September, and December to discuss what’s new with SCN8A. The Fast Inactivation Group is for individuals with the following variant locations: "p." number in one of the following ranges 1310-1325, 1466-1501, 1640-1654, 1760-1771. Please join us to learn more and meet other families with fast …
Our caregivers group meets the first Sunday of January, April, July, and October to discuss what's new with SCN8A and how we can best support our children. Please join us to learn more! Register here!
