家族性多形性室性心动过速中心脏兰尼碱受体（RyR2）基因的突变

Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

1. 1Decrease in myocardial ryanodine receptors and altered excitation-contraction coupling early in the development of heart failure.1994 · 107 citations
2. 2SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome1995 · 1,698 citations
3. 3Arrhythmic disorder mapped to chromosome 1q42–q43 causes malignant polymorphic ventricular tachycardia in structurally normal hearts1999 · 346 citations
4. 4The Locus of a Novel Gene Responsible for Arrhythmogenic Right-Ventricular Dysplasia Characterized by Early Onset and High Penetrance Maps to Chromosome 10p12-p142000 · 140 citations
5. 5Molecular cloning and characterization of a human brain ryanodine receptor¹1997 · 43 citations