QuickView for CACNB2;jsessionid=DBD61CA45A8F05E6B5DA177159229349;jsessionid=561A2269E8F6F50446EB15219665E0B0;jsessionid=4935D797333C42698D956B9202AC9A5B;jsessionid=F55BAE7CE8FDC892539AC4860BD86E8D;jsessionid=3CCE4F1D2F91149E3651D9E59D131BC0 (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=DBD61CA45A8F05E6B5DA177159229349;jsessionid=561A2269E8F6F50446EB15219665E0B0;jsessionid=4935D797333C42698D956B9202AC9A5B;jsessionid=F55BAE7CE8FDC892539AC4860BD86E8D;jsessionid=3CCE4F1D2F91149E3651D9E59D131BC0