QuickView for CACNB2;jsessionid=392F5E2B22D1A2EEB9A890E144CB6147;jsessionid=08A04B7096CBD5B3DF9B1B05F254442A;jsessionid=25486A887E9E5D740231EF0C925B8094;jsessionid=47DAA9E3356E657E7B6897DF3BEF17BE;jsessionid=7825CE8B2EB4778EEFD2E68FD6DD106B (gene)

1. A novel calcium channel Cavβ2 splice variant with unique properties predominates in the retina.
2. A Preclinical Study on Brugada Syndrome with a CACNB2 Variant Using Human Cardiomyocytes from Induce…
3. A Post-GWAS Functional Analysis Confirming Effects of Three BTA13 Genes CACNB2, SLC39A12, and ZEB1 o…
4. Active Zone Trafficking of CaV2/UNC-2 Channels Is Independent of β/CCB-1 and α2δ/UNC-36 Subunits.
5. Autism-associated mutations in the CaVβ2 calcium-channel subunit increase Ba2+-currents and lead to …

There were no clinical trials for CACNB2;jsessionid=392F5E2B22D1A2EEB9A890E144CB6147;jsessionid=08A04B7096CBD5B3DF9B1B05F254442A;jsessionid=25486A887E9E5D740231EF0C925B8094;jsessionid=47DAA9E3356E657E7B6897DF3BEF17BE;jsessionid=7825CE8B2EB4778EEFD2E68FD6DD106B