QuickView for CACNB2;jsessionid=0109C9A2A385BE0441E7C8FC826EBB44 (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=0109C9A2A385BE0441E7C8FC826EBB44