Unravelling Novel SCN5A Mutations Linked to Brugada Syndrome: Functional, Structural, and Genetic Insights

MLA

Frosio, A., et al. Unravelling Novel SCN5A Mutations Linked to Brugada Syndrome: Functional, Structural, and Genetic Insights. 2023. EBSCOhost, widgets.ebscohost.com/prod/customlink/proxify/proxify.php?count=1&encode=0&proxy=&find_1=&replace_1=&target=https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=edsoai&AN=edsoai.on1415731397&authtype=sso&custid=ns315887.

APA

Frosio, A., Micaglio, E., Polsinelli, I., Calamaio, S., Melgari, D., Prevostini, R., Ghiroldi, A., Binda, A., Carrera, P., Villa, M., Mastrocinque, F., Presi, S., Salerno, R., Boccellino, A., Anastasia, L., Ciconte, G., Ricagno, S., Pappone, C., Rivolta, I., … Rivolta I. (2023). Unravelling Novel SCN5A Mutations Linked to Brugada Syndrome: Functional, Structural, and Genetic Insights.

Chicago

Frosio, A, E Micaglio, I Polsinelli, S Calamaio, D Melgari, R Prevostini, A Ghiroldi, et al. 2023. “Unravelling Novel SCN5A Mutations Linked to Brugada Syndrome: Functional, Structural, and Genetic Insights.” http://widgets.ebscohost.com/prod/customlink/proxify/proxify.php?count=1&encode=0&proxy=&find_1=&replace_1=&target=https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=edsoai&AN=edsoai.on1415731397&authtype=sso&custid=ns315887.