Associated Papers
Multiomic and electrophysiologic analyses reveal that an inherited MRC2 variant causes fibroblast dysfunction and increased atrial fibrillation susceptibility.
Ho KS et al.
American Journal of Physiology. Heart and Circulatory Physiology, 2025
Rare Variant in MRC2 Associated With Familial Supraventricular Tachycardia and Wolff-Parkinson-White Syndrome.
Potter AS et al.
Circulation. Genomic and Precision Medicine, 2024
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