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.

@inflames-flagship.bsky.social @curesyngap1.bsky.social
@turkubioscience.bsky.social
https://www.utu.fi/en/news/press-release/researchers https://bsky.app/profile/utu.fi/post/3lmjhl2ewek2z #utu #yliopisto

Harvinaisen lasten kehityshäiriön tutkimus Turun yliopistossa saa jatkoa uusien rahoitusten tuella. Tutkijoidemme kohteena on sairaus, joka aiheuttaa moninaisia ja vakavia hermostollisia oireita.

#SynGAP1 #NSID

@inflames-flagship.bsky.social @curesyngap1.bsky.social
https://www.utu.fi/fi/ajankohtaista/mediatiedote/turun-yliopiston-tutkijoille-l https://bsky.app/profile/utu.fi/post/3lmjgz3ae3c2z #utu #yliopisto

SynGAP1 is a crucial protein in neuronal development and the mutations in the SynGAP1 gene lead to Non-Syndromic Intellectual Disability, #NSID. With new funding, our researchers will continue to study this challenging disease, which often starts in childhood.

@turkubioscience.bsky.social
https://inflames.utu.fi/researchers-secure-funding-to-stud https://bsky.app/profile/inflames-flagship.bsky.social/post/3lmewusce4c2d #utu #yliopisto