Review
Open access
Jan 2026
Rare Variants in Purinergic P2X Receptor Genes (P2RX4, P2RX5, P2RX7) in Individuals With Autism Spectrum Disorder: An Exploratory Study
Preliminary, exploratory observations suggesting that rare P2RX variants may represent biologically plausible candidates relevant to ASD‐related pathways are provided; however, no conclusions regarding disease association or causality can be drawn.
Gül Ünsel-Bolat, H. Bolat
· Human Mutation · 0 citations