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HARVARD Citation
Kovacs, B. et al. (2021). A novel variant in the SLC4A3 gene with high penetrance in a family with short QT Syndrome. Europace. p. . [Online].
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Kovacs, B. et al. (2021). A novel variant in the SLC4A3 gene with high penetrance in a family with short QT Syndrome. Europace. p. . [Online].