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Published in 2023 at "Europace"
DOI: 10.1093/europace/euad122.601
Abstract: Abstract Funding Acknowledgements Type of funding sources: None. Background Rare variants in the SCN5A gene have been associated with Brugada syndrome (BS), long QT syndrome type 3 (LQTS3), and other conduction disorders that can lead…
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Keywords:
rare variants;
scn5a gene;
variants scn5a;
phenotype correlation ... See more keywords