LAUSR

COMPOUND SCN5A MUTATION AND FGF12 VARIATION CAUSE BRUGADA SYNDROME

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0 Published in 2017 at "Journal of the American College of Cardiology"

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