Pub. Date : 2020 Jul
PMID : 32115705
1 Functional Relationships(s)Download |
Sentence | Compound Name | Protein Name | Organism |
| 1 | At present, mutations in six genes involved in SR calcium release have been identified as the genetic cause of CPVT: RYR2 (encoding ryanodine receptor calcium release channel), CASQ2 (encoding cardiac calsequestrin), TRDN (encoding triadin), CALM1, CALM2 and CALM3 (encoding identical calmodulin protein). | Calcium | triadin | Homo sapiens |