Embryonic type Na+ channel β-subunit, SCN3B masks the disease phenotype of Brugada syndrome.
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, Aiba T, Shimizu W, Horie M, Kamiya K, Furukawa T, Fukuda K.
Okata S, et al. Among authors: tanaka a.
Sci Rep. 2016 Sep 28;6:34198. doi: 10.1038/srep34198.
Sci Rep. 2016.
PMID: 27677334
Free PMC article.