Collection for Louis Angelinetta's Leaving Do for SYNGAP1 research at the Patrick Wild Centre in memory of James Nash
on 16 June 2022
on 16 June 2022
With the passing of our good friend and colleague James Nash, Louis has asked that any collections towards his leaving do be donated to a charity close to James and Jo's heart - SynGap1 research
After 15yrs in the same building, having worked for 3 different companies in multiple roles and working his way up the corporate ladder Louis has decided to move on to different pastures. Louis will be sorely missed and we wish him all the best with his new adventure.
A SYNGAP1 gene mutation can cause a variety of symptoms that can range from mild to severe. The most common symptoms include learning difficulties, epilepsy, behavioural challenges, autism, and sensory processing disorder. Research is vital.
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