IndraLab

Statements

SCN5A activates SCD. 3 / 3
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"Interestingly, mutations in SCN5A also cause DCM, a main cause of SCD."
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"Taking together, the identified SCN5A p. 1493delK mutation leads to CCD, ventricular arrhythmias and SCD, in the absence of signs of BrS or LQTS."
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"Mutations in the DPP6 gene have been previously associated with the development of idiopathic ventricular fibrillation (IVF), which is known to cause SCD [14]."
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