Where I see patients (2)
Selected research
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ALPK3 Heterozygous Truncating Variants Cause Late-Onset Hypertrophic Cardiomyopathy With Frequent Apical Involvement and Apical Aneurysm.
Circulation. Genomic and precision medicine
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Molecular convergence of risk variants for congenital heart defects leveraging a regulatory map of the human fetal heart.
medRxiv : the preprint server for health sciences
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Transcriptomic Profiling of Human Myocardium at Sudden Death to Define Vulnerable Substrate for Lethal Arrhythmias.
JACC. Clinical electrophysiology