IndraLab

Statements



sparser
"Variants in CACNA1C (Cav1.2), CACNB2b (CavB2b) and CACNA2D1 (Cavα2δ) have been reported in up to 13% of probands. [ xref – xref ] Mutations in glycerol-3-phophate dehydrogenase 1- like enzyme gene (GPD1L), SCN1B (β1-subunit of Na channel), KCNE3 (MiRP2), SCN3B (β3- subunit of Na channel), KCNJ8 (Kir6.1), KCND3 (Kv4.3), RANGRF (MOG1), SLMAP, ABCC9 (SUR2A), SNC2B (Navβ2), PKP2 (Plakophillin-2), FGF12 (FHAF1), HEY2, and SEMA3A (Semaphorin) are relatively rare.[ xref – xref ] An association of BrS with SCN10A, a neuronal sodium channel, was recently reported.[ xref , xref ]"

sparser
"An association of BrS with SCN10A , a neuronal sodium channel, was recently reported xref , xref , xref ."