Connecting European Neuroscience

Syngap1 and related disorders

Dates
March 15th, 2021 to March 16th, 2021
Venue
Vienna, Austria

Brain Disease, Brain Development, Synapses

About the Event

Syngap1 is a protein that is critical for the development of cognition and proper synapse function. Mutations in the Syngap1 gene lead to a rare neurodevelopmental disorder. Currently, about 400 children are diagnosed world-wide with this disease. Mutations in Syngap1 are associated with intellectual disability and are proposed to play a significant role in other diseases such as epilepsy, autism spectrum disorders and schizophrenias.

Contact

Sigismund Huck
Spitalgasse 4

Phone:+43 (0)1 40160-34090
Email:sigismund.huck@meduniwien.ac.at
Website:https://syngap-symposium.com/

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