SynGAP1 is a crucial protein in neuronal development. Mutations in the SynGAP1 gene lead to Non-Syndromic Intellectual Disability #NSID. Our researchers have secured funding to study this rare disease further.

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@turkubioscience.bsky.social
https://www.utu.fi/en/news/press-release/researchers https://bsky.app/profile/utu.fi/post/3lmjhl2ewek2z #utu #yliopisto