Overcôme Syngap1 aims at raising awareness on the SYNGAP1 genetic disorder, helping families affected by the disease and raising funds to find a cure.
Mutations of the SYNGAP1 gene in humans can cause intellectual disability and/or epilepsy. This gene is also related to autism.
Our organization presently funds:
– a research project with the Ste Justine Hospital unit in Montréal, Canada (Professor Michaud team)
– a research project with the Interdisciplinary Institute of Neurosciences (IINS) in Bordeaux, France (Professor Choquet team).
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Find out about our global network: https://www.syngapglobal.net/

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