Associated Papers
Novel SCN5A variants identified in a group of Iranian Brugada syndrome patients.
Ghaffari T et al.
Functional & Integrative Genomics, 2021
Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls.
Walsh R et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2021
32893267 (PubMed )
Supplement: 41436_2020_946_MOESM2_ESM.xlsx › S3
Actionable Pharmacogenetic Variation in the Slovenian Genomic Database.
Hočevar K et al.
Frontiers in Pharmacology, 2019
30930780 (PubMed )
Supplement: Table_5.xlsx › Sheet1
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