QuickView for NRXN3;jsessionid=82CD544AD1499287A6C08BAED0132DC2;jsessionid=02EC54BF020E2DFDAF5F52B927912364;jsessionid=068CCF540AC9F48A62DCBB1BD1F1599A;jsessionid=6759138094C493C47E342A0B63B9CC69;jsessionid=8FB0B465DDA9D50368AECE0090A85C0E;jsessionid=D3CC7F3116CB86D56E1FF206CFF68D32 (gene)

1. NRXN3 mutations cause developmental delay, movement disorder, and behavioral problems: CRISPR edited…
2. A combinatorial code of neurexin-3 alternative splicing controls inhibitory synapses via a trans-syn…
3. Neurexin-3 subsynaptic densities are spatially distinct from Neurexin-1 and essential for excitatory…
4. Neurexin-3 defines synapse- and sex-dependent diversity of GABAergic inhibition in ventral subiculum…
5. Distinct neurexin isoforms cooperate to initiate and maintain foraging activity.

There were no clinical trials for NRXN3;jsessionid=82CD544AD1499287A6C08BAED0132DC2;jsessionid=02EC54BF020E2DFDAF5F52B927912364;jsessionid=068CCF540AC9F48A62DCBB1BD1F1599A;jsessionid=6759138094C493C47E342A0B63B9CC69;jsessionid=8FB0B465DDA9D50368AECE0090A85C0E;jsessionid=D3CC7F3116CB86D56E1FF206CFF68D32