IndraLab

Statements

SCN5A binds TPS-sab. 3 / 3
| 3
sparser
"The overlap of SSS and gain-of-function mutations associated with LQT3 is more complex."
30327767
sparser
"There have been 13 previous SCN5A mutations associated with familial SSS by itself or in combination with BrS or LQTS have thus far been identified."
18616619
sparser
"Six heterozygous SCN5A mutations have been associated with an autosomal recessive congenital SSS with complete penetrance also associated with conduction disorders including evidence for latent atrioventricular conduction system disease."
18616619