COMPOUND SCN5A MUTATION AND FGF12 VARIATION CAUSE BRUGADA SYNDROME
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DOI: 10.1016/s0735-1097(17)33721-x
Abstract: Background: Mutations in the voltage-gated sodium channel (SCN5A; Nav1.5) and its regulating genes, such as fibroblast growth factor 12 (FGF12), are linked to Brugada syndrome (BrS). The goal of this study is to identify additional… read more here.
Keywords: compound scn5a; mutation fgf12; fgf12 variation; brugada syndrome ... See more keywords