The main ongoing research is represented by:
• Project “Understanding AP1S2-related disorders” by ITHACA (https://ern-ithaca.eu/our-research-activities/calls-for-collaboration/understanding-ap1s2-related-disorders/): Multicentre retrospective collection of clinical, EEG and neuroimaging data of patients carrying mono-allelic loss-of-function variants in AP1S2 (coordinator Allan Bayat abaya@filadelfia.dk or bayabayabayat@hotmail.com, Department of Pediatrics, Danish Epilepsy Centre, Filadelfia)
AP1S2