Associated Papers
A Novel Loss-of-Function Variant in the Chloride Ion Channel Gene Clcn2 Associates with Atrial Fibrillation.
Hansen TH et al.
Scientific Reports, 2020
31996765 (PubMed )
Supplement: 41598_2020_58475_MOESM1_ESM.pdf
Pediatric Malignant Arrhythmias Caused by Rare Homozygous Genetic Variants in TRDN: A Comprehensive Interpretation.
Sarquella-Brugada G et al.
Frontiers in Pediatrics, 2020
Select a paper to view details