RYR2
ryanodine receptor 2
Ассоциированные заболевания
Герминативная мутация (причина)4
Catecholaminergic polymorphic ventricular tachycardiaORPHA:3286
→Inherited isolated arrhythmogenic cardiomyopathy, dominant-right variantORPHA:293910
→Inherited isolated arrhythmogenic ventricular dysplasia, biventricular variantORPHA:293899
→Inherited isolated arrhythmogenic cardiomyopathy, dominant-left variantORPHA:293888
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