QuickView for P2RX2;jsessionid=9383B5C7EAB5D944DBF9E191B9EA1C89 (gene)

1. Generation and characterization of a P2rx2 V60L mouse model for DFNA41.
2. Identification of a Novel Stop Loss Mutation in P2RX2 Gene in an Iranian Family with Autosomal Nonsy…
3. Characterization of UMi028-A-1 stem cell line that contains a CRISPR/Cas9 induced hearing loss-assoc…
4. Disruption of hippocampal P2RX2/CaMKII/NF-κB signaling contributes to learning and memory impairment…
5. Progressive Dominant Hearing Loss (Autosomal Dominant Deafness-41) and P2RX2 Gene Mutations: A Pheno…

There were no clinical trials for P2RX2;jsessionid=9383B5C7EAB5D944DBF9E191B9EA1C89