Embryonic type Na+ channel β-subunit, SCN3B masks the disease phenotype of Brugada syndrome.

MLA

Okata, Shinichiro, et al. “Embryonic Type Na+ Channel β-Subunit, SCN3B Masks the Disease Phenotype of Brugada Syndrome.” Scientific Reports, Sept. 2016, p. 34198. EBSCOhost, https://doi.org/10.1038/srep34198.

APA

Okata, S., Yuasa, S., Suzuki, T., Ito, S., Makita, N., Yoshida, T., Li, M., Kurokawa, J., Seki, T., Egashira, T., Aizawa, Y., Kodaira, M., Motoda, C., Yozu, G., Shimojima, M., Hayashiji, N., Hashimoto, H., Kuroda, Y., Tanaka, A., & Murata, M. (2016). Embryonic type Na+ channel β-subunit, SCN3B masks the disease phenotype of Brugada syndrome. Scientific Reports, 34198. https://doi.org/10.1038/srep34198

Chicago

Okata, Shinichiro, Shinsuke Yuasa, Tomoyuki Suzuki, Shogo Ito, Naomasa Makita, Tetsu Yoshida, Min Li, et al. 2016. “Embryonic Type Na+ Channel β-Subunit, SCN3B Masks the Disease Phenotype of Brugada Syndrome.” Scientific Reports, September, 34198. doi:10.1038/srep34198.