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 Identification of a Novel SCN5A  gene variant in a young female with atrioventricular canal defect in the absence of classical Brugada syndrome phenotype.
<strong>Medical Research Archives</strong>, [S.l.], v. 12, n. 7, july 2024.
ISSN 2375-1924.
Available at: &lt;<a href="https://esmed.org/MRA/mra/article/view/5527" target="_new">https://esmed.org/MRA/mra/article/view/5527</a>&gt;. Date accessed: 22 dec. 2024.
doi: <a href="https://doi.org/10.18103/mra.v12i7.5527">https://doi.org/10.18103/mra.v12i7.5527</a>.