PO-629-03 IN-DEPTH ANALYSIS OF THE SCN5A LOCUS HIGHLIGHTS DISTINCT GENETIC ARCHITECTURES FOR BRUGADA SYNDROME IN DIFFERENT ANCESTRIES AND IDENTIFIES A NOVEL RARE ENHANCER VARIANT ASSOCIATED WITH DISEASE IN SOUTHEAST ASIAN PATIENTS.

MLA

Walsh, Roddy, et al. “Po-629-03 In-Depth Analysis of the Scn5a Locus Highlights Distinct Genetic Architectures for Brugada Syndrome in Different Ancestries and Identifies a Novel Rare Enhancer Variant Associated with Disease in Southeast Asian Patients.” Heart Rhythm, vol. 19, no. 5, May 2022, pp. S161–62. EBSCOhost, https://doi.org/10.1016/j.hrthm.2022.03.888.

APA

Walsh, R., Khongphatthanayothin, A., Mauleekoonphairoj, J., Beekman, L., Kooyman, M., Wu, C.-I., Barc, J., Tadros, R., Amin, A. S., Postema, P. G., Wijeyeratne, Y. D., Lambiase, P. D., Behr, E., Wilde, A. A. M., Poovorawan, Y., Bezzina, C. R., & Nademanee, K. (2022). Po-629-03 In-Depth Analysis of the Scn5a Locus Highlights Distinct Genetic Architectures for Brugada Syndrome in Different Ancestries and Identifies a Novel Rare Enhancer Variant Associated with Disease in Southeast Asian Patients. Heart Rhythm, 19(5), S161–S162. https://doi.org/10.1016/j.hrthm.2022.03.888

Chicago

Walsh, Roddy, Apichai Khongphatthanayothin, John Mauleekoonphairoj, Leander Beekman, Maarten Kooyman, Cheng-I Wu, Julien Barc, et al. 2022. “Po-629-03 In-Depth Analysis of the Scn5a Locus Highlights Distinct Genetic Architectures for Brugada Syndrome in Different Ancestries and Identifies a Novel Rare Enhancer Variant Associated with Disease in Southeast Asian Patients.” Heart Rhythm 19 (5): S161–62. doi:10.1016/j.hrthm.2022.03.888.