[HTML][HTML] Key roles of C2/GAP domains in SYNGAP1-related pathophysiology

D Katsanevaki, SM Till, I Buller-Peralta, MS Nawaz… - Cell Reports, 2024 - cell.com
Mutations in SYNGAP1 are a common genetic cause of intellectual disability (ID) and a risk
factor for autism. SYNGAP1 encodes a synaptic GTPase-activating protein (GAP) that has …