Open AccessCalmodulinopathy in inherited arrhythmia syndromes
Author(s) -
Wen-Chin Tsai,
PengSheng Chen,
Michael Rubart
Publication year - 2021
Publication title -
tzu-chi medical journal/cí-jì yīxué
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 0.343
H-Index - 15
eISSN - 2223-8956
pISSN - 1016-3190
DOI - 10.4103/tcmj.tcmj_182_20
Subject(s) - catecholaminergic polymorphic ventricular tachycardia , medicine , sudden cardiac death , long qt syndrome , ryanodine receptor 2 , cardiac arrhythmia , sudden death , phenotype , mutation , gene , calmodulin , channelopathy , bioinformatics , genetics , neuroscience , qt interval , biology , calcium , ryanodine receptor , atrial fibrillation