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Paper Details

Loss-of-Function <i>FLNC</i> Variants Are Associated With Arrhythmogenic Cardiomyopathy Phenotypes When Identified Through Exome Sequencing of a General Clinical Population.
Circ Genom Precis Med
9
2022
Arrhythmogenic Cardiomyopathy, arrhythmogenic cardiomyopathy, dilated cardiomyopathy, genetic condition, left-dominant arrhythmogenic cardiomyopathy, patients, supraventricular tachycardia, ventricular arrhythmia
Author NameAffiliation
Amy C SturmThe Heart Institute (M.Q.
Amy C SturmGenomic Medicine Institute (M.A.K.
Aris Baras
Cynthia A JamesJohns Hopkins Medical Center
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Release 1.2